N-Aryl-2-oxazolidinone-5-carboxamides and their derivatives

ABSTRACT

The present invention provides antibacterial agents having the formula I described herein.

CROSS REFERENCE TO RELATED APPLICATIONS

[0001] This application claims the benefit of U.S. Provisional Application Serial No., 60/428,025, filed, Nov. 21, 2002, and U.S. Provisional Application Serial No., 60/445,530, filed, Feb. 6, 2003, both of which are incorporated herein by reference in their entireties.

FIELD OF INVENTION

[0002] The present invention relates to novel N-Aryl-2-oxazolidinone-5-carboxamides, derivatives thereof, and their preparations. These compounds have potent antibacterial activity.

BACKGROUND OF THE INVENTION

[0003] The oxazolidinone antibacterial agents are a novel synthetic class of antimicrobials with potent activity against a number of human and veterinary pathogens, including Gram-positive aerobic bacteria such as multiply-resistant staphylococci and streptococci, anaerobic organisms such as bacteroides and clostridia species, and acid-fast organisms such as Mycobacterium tuberculosis and Mycobacterium avium.

SUMMARY OF THE INVENTION

[0004] In one aspect, the invention features compounds of Formula I.

[0005] or pharmaceutically acceptable salts thereof wherein:

[0006] A is a structure i, ii, iii, or iv;

[0007] W is —N(H)C(X)—R₁, Het, or —Y—HET, in which the Het or —Y—HET is optionally substituted with ═S or ═O, provided that when A is structure iv, W is not —Y—HET or Het;

[0008] X is O or S;

[0009] Y is NH, O, or S;

[0010] R₁ is a) H,

[0011] b) NH₂,

[0012] c) NHC₁₋₄alkyl,

[0013] d) C₁₋₄ alkyl,

[0014] e) C₂₋₄ alkenyl,

[0015] f) O—C₁₋₄ alkyl,

[0016] g) S—C₁₋₄alkyl, or

[0017] h) (CH₂)_(s) C₃₋₆ cycloalkyl, in which each occurrence of alkyl or cycloalkyl in R₁ is optionally substituted by one, two or three halogens (F or Cl);

[0018] Each R₂ and R₃ is independently hydrogen, halogen (F or Cl), methyl or ethyl;

[0019] R₄ is H, CH₃ or F;

[0020] R₅ is H or C₁₋₄ alkyl;

[0021] R₆ is H, C₁₋₄ alkyl, or

[0022] or R₅ and R₆ together form an optionally substituted saturated heterocycle;

[0023] R₇ is H, or C₁₋₄ alkyl which can be optionally substituted by —OH, —NH₂, —NH—C(═NH)—NH₂, —SH, —SCH₃, —COOH, —C(O)NH₂, phenyl which can be optionally substituted with —OH;

[0024] R₈ is H or CH₃;

[0025] R₉ is H, CH₃, —C(O)—CH(R₇)—NR₈R₈,

[0026] R₁₀ or R₁₁ is halo, C₁₋₄alkyl, CF₃, —CN, —NO₂, —OH, —O—C₁₋₄alkyl, —NH—S(O)_(w)C₁₋₄alkyl;

[0027] R₁₂ is H, C₁₋₄alkyl, —S(O)₂—C₁₋₄alkyl,

[0028] or R₅ and R₁₂ together form a saturated heterocycle;

[0029] R₁₃ is H, or

[0030] R₁₄ is —(CH₂)_(t)NHR₁₃, —OH, —OC₁₋₄alkyl;

[0031] m is 0, 1, 2, 3, 4;

[0032] n is 0, 1, 2, 3, 4 with the proviso that m plus n is 2, 3, 4, or 5;

[0033] p is 2, 3;

[0034] q is 1, 2;

[0035] r, s and t are independently 0, 1;

[0036] u and w are independently 0, 1, 2; and

[0037] provided that W is not Het or —Y—HET when Z is a, b, or d, and further provided that Z is not b when A is formula iii.

[0038] Embodiments of the invention may have one or more of the following. R₁₀ is CF₃. R₁₁ is CF₃. Heterocycle is piperidino, pyrrolidino, morpholino, thiomorpholino, or 4-methyl-1-piperazinyl. Het is a triazole or a tetrazole. B is

[0039] p is 2. B is

[0040] n and m are both 2. n and m are both 1. R₄ is —CH₃. Z is (a). R₅ and R₆ are C₁₋₄ alkyl. R₅ and R₆ together form an optionally substituted saturated heterocycle. R₅ and R₆ form an optionally substituted morpholinyl and piperazinyl. R₅ and R₆ form a morpholinyl and piperazinyl each of which are substituted with C₁₋₄ alkyl. u=0. Z is (c). R₁₀ is H. R₁₁ is —C(O)—NH₂, —NHS(O)_(u),C₁₋₄alkyl, or —(CH₂)_(t)—NR₅R₁₂. R₁₁ is —CH₂N(C₁₋₄alkyl)₂, —CH₂-saturated heterocycle, —CH₂—NH—C₁₋₄alkyl, —CH₂—N(C1-4alkyl)-C(O)—CHR₇—NR₈R₉, —CH₂—NH—C(O)—C₁₋₄alkyl, —CH₂—NH—SO₂—(C1-4alkyl), —CH₂—NH₂, or —NH—C(O)—CHR₇—NR₈R₉. R₁₀ is ortho to R₁₁. q is 1. Z is (b). R₁₄ is —OC₁₋₄ alkyl, —OH, or —NH—C(O)—CH(R₇)—NR₈R₉.

[0041] In another aspect, the invention features a method for the treatment of microbial infections in mammals by administering an effective amount of compound of formula I to a mammal. The compound may be administered to the mammal orally, parenterally, transdermally, or topically. The compound may be part of a pharmaceutical composition. The compound may be administered in an amount of from about 0.1 to about 100 mg/kg of body weight/day, e.g., from about 1 to about 50 mg/kg of body weight/day.

[0042] In another aspect, the invention features a pharmaceutical composition including a compound of claim 1 and a pharmaceutically acceptable carrier.

[0043] Specific compounds of the invention include:

[0044] N-[((5S)-3-{4-[4-({4-[(Diethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide.

[0045] N-[((5S)-3-{4-[4-({4-[(Diethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]cyclopropanecarbothioamide.

[0046] N-[((5S)-3-{4-[4-({4-[(Diethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide.

[0047] N-[((5S)-3{4-[4-({4-[(Dimethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide.

[0048] N-[((5S)-3-{4-[4-({4-[(Dimethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]cyclopropanecarbothioamide.

[0049] N-[((5S)-3-{4-[4-({4-[(Dimethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide.

[0050] N-({(5S)-3-[3-Fluoro-4-(4-{[4-(morpholin-4-ylmethyl)phenoxy]acetyl}piperazin-1-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)propanethioamide.

[0051] N-({(5S)-3-[3-Fluoro-4-(4-{[4-(morpholin-4-ylmethyl)phenoxy]acetyl}piperazin-1-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)cyclopropanecarbothioamide.

[0052] N-({(5S)-3-[3-Fluoro-4-(4-{[4-(morpholin-4-ylmethyl)phenoxy]acetyl}piperazin-1-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide.

[0053] N-[((5S)-3-{3-Fluoro-4-[4-({4-[(4-methylpiperazin-1-yl)methyl]phenoxy}acetyl)piperazin-1-yl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide.

[0054] N-[((5S)-3-{3-Fluoro-4-[4-({4-[(4-methylpiperazin-1-yl)methyl]phenoxy}acetyl)piperazin-1-yl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]cyclopropanecarbothioamide (38)

[0055] N-[((5S)-3-{3-Fluoro-4-[4-({4-[(4-methylpiperazin-1-yl)methyl]phenoxy}acetyl)piperazin-1-yl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide.

[0056] N-[((5S)-3-{4-[4-(4-{4-[(Dimethylamino)methyl]phenyl}-4-oxobutanoyl)-1-piperazinyl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide.

[0057] N-[((5S)-3-{4-[4-(4-{4-[(Dimethylamino)methyl]phenyl}-4-oxobutanoyl)-1-piperazinyl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]cyclopropanecarbothioamide.

[0058] N-[((5S)-3-{4-[4-(4-{4-[(Dimethylamino)methyl]phenyl}-4-oxobutanoyl)-1-piperazinyl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide.

[0059] N-({(5S)-3-[3-Fluoro-4-(4-{4-[4-(4-morpholinylmethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)propanethioamide.

[0060] N-({(5S)-3-[3-Fluoro-4-(4-{4-[4-(4-morpholinylmethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide.

[0061] N-({(5S)-3-[3-Fluoro-4-(4-{4-[4-(4-morpholinylmethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)cyclopropanecarbothioamide.

[0062] N-[((5S)-3-{3-Fluoro-4-[4-(4-{4-[(methylamino)methyl]phenyl}-4-oxobutanoyl)piperazin-1-yl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide.

[0063] N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-piperazin-1-yl]-4-oxobutanoyl}benzyl-N¹-methylglycinamide.

[0064] N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)-N¹,N²,N²-trimethylglycinamide.

[0065] N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)-N²,N²-dimethylglycinamide.

[0066] N¹-(4-{4-[4-[2-Fluoro-4-{(5S)-2-oxo-5-[(propanethiolylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)-N²,N²-dimethylglycinamide.

[0067] (S)—N¹-(4-{4-[4-(2-Fluoro-4-{(5S)-2-oxo-5-[(propanethioylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)alaninamide.

[0068] (S)—N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3yl}-2-fluorophenyl)piperazin-1-yl]-2-oxobutanoyl}benzyl)alaninamide.

[0069] N¹-(4-{4-[4-(2-Fluoro-4-{(5S)-2-oxo-5-[(propanethioylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)glycinamide.

[0070] (S)-Alanyl-(S)—N¹-(4-{4-[4-(2-fluoro-4-{(5S)-2-oxo-5-[(propanethioylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)alaninamide.

[0071] (S)-Alanyl-(S)—N¹-(4-{4-[4-(4-{(5S)-5-[(acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl }-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)alaninamide.

[0072] N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}benzyl)acetamide.

[0073] N-(4-{4-[4-(2-Fluoro-4-{(5S)-2-oxo-5-[(propanethioylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)-1-piperazinyl]-4-oxobutanoyl}benzyl)acetamide.

[0074] N-{[(5S)-3-(3-Fluoro-4-{4-[4-(4-{[(methylsulfonyl)amino]methyl}phenyl)-4-oxobutanoyl]-1-piperazinyl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide.

[0075] N-{[(5S)-3-(3-Fluoro-4-{4-[4-(4-{[(methylsulfonyl)amino]methyl}phenyl)-4-oxobutanoyl]-1-piperazinyl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}propanethioamide.

[0076] N-({(5S)-3-[4-(4-{4-[4-(Aminomethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl)-3-fluorophenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)propanethioamide.

[0077] N-({(5S)-3-[4-(4-{4-[4-(Aminomethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl)-3-fluorophenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide.

[0078] N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)glycinamide.

[0079] 2-[3-methyl-3-(4-{(5S)-2-oxo-5-[(propionylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)azetidin-1-yl]-2-oxoethyl 4-(aminomethyl)benzamide.

[0080] N-{[(5S)-3-(4-{1-[4-(4-aminophenyl)-4-oxobutanoyl]-3-methylazetidin-3-yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}propanamide.

[0081] N-({(5S)-3-[4-(1-{4-[4-(glycylamino)phenyl]-4-oxobutanoyl}-3-methylazetidin-3-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)propanamide.

[0082] N-{[(5S)-3-(4-{1-[4-(4-aminophenyl)-4-oxobutanoyl]-3-methylazetidin-3-yl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide.

[0083] N˜1˜-(4-{4-[3-(4-{(5S)-5-[(acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-3-methylazetidin-1-yl]-4-oxobutanoyl}phenyl)glycinamide.

[0084] 2-[3-(4-{(5S)-5-[(acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-3-methylazetidin-1-yl]-2-oxoethyl-4-(aminomethyl)benzamide.

[0085] N-{[(5S)-3-(3-Fluoro-4-{4-[4-(4-methoxyphenyl)butanoyl]piperazine-1-yl}phenyl)2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide.

[0086] N-{[(5S)-3-(3-Fluoro-4-{4-[4-(4-hydroxyphenyl)butanoyl]piperazin-1-yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide.

[0087] 2,2-Difluoro-N-{[(5S)-3-(3-fluoro-4-{4-[4-(4-methoxyphenyl)butanoyl]piperazin-1-yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}ethanethioamide.

[0088] N-{[(5S)-3-(4-{4-[4-(4-Bromophenyl)-4-oxobutanoyl]-1-piperazinyl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide.

[0089] N-{[(5S)-3-(4-{4-[4-(4-Bromophenyl)-4-oxobutanoyl]-1-piperazinyl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}ethanethioamide.

[0090] N-{[(5S)-3-(4-{4-[4-(4-Cyanophenyl)-4-oxobutanoyl]-1-piperazinyl}-3-fluorophenyl-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide.

[0091] 4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}benzamide.

[0092] 4-{4-[4-(4-{(5S)-5-[(Ethanethiolylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}benzamide.

[0093] N-{[(5S)-3-(4-{4-[4-(4-Chlorophenyl)-4-oxobutanoyl]-1-piperazinyl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide.

[0094] N-{[(5S)-3-(4-{4-[4-(4-chlorophenyl)-4-oxobutanoyl]-1-piperazinyl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}ethanethioamide.

[0095] N-[((5S)-3-{3-Fluoro-4-[4-(4-{4-[(methylsulfonyl)amino]phenyl}-4-oxobutanoyl)-1-piperazinyl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide.

[0096] N-[((5S)-3-{3-Fluoro-4-[4-(4-{4-[(methylsulfonyl)amino]phenyl}-4-oxobutanoyl-1-piperazinyl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide. N-(4-{4-[4-(2-Fluoro-4-{(5S)-2-oxo-5-[(propanethiolylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)-1-piperazinyl]-4-oxobutanoyl}phenyl)acetamide.

[0097] 2-Amino-N-(4-{4-[4-(2-fluoro-4-{(5S)-2-oxo-5-[(propanethiolylamino)methyl]1,3-oxazolidin-3-yl}phenyl)-1-piperazinyl]-4-oxobutanoyl}phenyl)acetamide.

[0098] N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}phenyl)-2-aminoacetamide.

[0099] N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}phenyl)-(2S)-2-aminopropanamide.

[0100] N-1-(4-{4-[4-(4-{(5S)-5-[(Ethanethiolylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}phenyl)-(S)-alaninamide.

[0101] N¹-[4-(5-{4-[4-((5S)-5-{[(2,2-Difluoroethanethioyl)amino]methyl}-2-oxo-1,3-oxazolidin-3-yl)-2-fluorophenyl]piperazin-1-yl}-5-oxopentanoyl)phenyl]glycinamide.

[0102] N¹-(4-{5-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-5-oxopentanoyl}phenyl)glycinamide.

[0103] N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutyl}phenyl)-2-aminoacetamide.

[0104] 2-Amino-N-(4-{4-[4-(2-fluoro-4-{(5S)-2-oxo-5-[(propanethiolylamino)methyl}-3-oxazolidin-3-yl}phenyl)-1-piperazinyl]-4-oxobutyl}phenyl)acetamide.

[0105] (S)-2-Amino-N-(4-{4-[4-(2-fluoro-4-{(5S)-2-oxo-5-[(propanethiolylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)-1-piperazinyl]-4-oxobutyl}phenyl)propanamide.

[0106] N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutyl)phenyl)-2-(dimethylamino)acetamide.

[0107] N-(4-{4-[4-(4-{(5S)-5-[(Ethanethiolylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutyl}phenyl)-2-(dimethylamino)acetamide

[0108] N¹-(3-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-1-hydroxy-4-oxobutyl}phenyl)glycinamide.

[0109] N¹-[3-(4-{4-[4-((5S)-5-{[(2,2-Difluoroethanethiolyl)amino]methyl}-2-oxo-1,3-oxazolidin-3-yl)-2-fluorophenyl]piperazin-1-yl}-4-oxobutanoyl)phenyl]glycinamide.

[0110] N-{[(5S)-3-(3-Fluoro-4-{4-[4-(3-nitrophenyl)-4-oxobutanoyl]piperazin-1yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}actamide.

[0111] N¹-(3-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}phenyl)glycinamide.

[0112] N-{[(5S)-3-(4-{4-[4-(2-Aminophenyl)-4-oxobutanoyl]piperazin-1-yl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide.

[0113] N-{[(5S)-3-(4-{4-[(5-Amino-1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)acetyl]piperazin-1-yl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide.

[0114] N¹-(2-{2-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl{-2fluorophenyl)piperazin-1-yl]-2-oxoethyl}-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl)glycinamide.

[0115] N¹-[2-(3-{4-[4-((5S)-5-{[(2,2-Difluoroethanethiolyl)amino]methyl}-2-oxo-1,3-oxazolidin-3-yl)-2-fluorophenyl]piperazin-1-yl}-3-oxopropyl)-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl)glycinamide.

[0116] Compounds of Formula I have antibacterial activity against a number of human and veterinary pathogens including Gram-positive aerobic bacteria such as multiply-resistant-staphylococci, streptococci and enterococci, Gram-negative organisms such as H. influenzae and M. catarrhalis, anaerobic organisms such as Bacteroides spp. and clostridia spp., Mycobacterium tuberculosis, M. avium and M. spp. and in organisms such as Mycoplasma spp. For use as antibacterial agents the compounds of this invention can be administered orally or parenterally in a dosage range of about 0.1-100 mg/kg or preferably of about 1.0-50 mg/kg of body weight per day. Advantageously, the compound of the invention exhibit antibacterial activity against S. aureus resistant organisms.

DETAILED DESCRIPTION OF THE INVENTION

[0117] The following definitions are used, unless otherwise described.

[0118] The carbon atom content of various hydrocarbon-containing moieties is indicated by a prefix designating the minimum and maximum number of carbon atoms in the moiety, i.e., the prefix C_(i-j) indicates a moiety of the integer “i” to the integer “j” carbon atoms, inclusive. Thus, for example, C₁₋₇ alkyl refers to alkyl of one to seven carbon atoms, inclusive.

[0119] The term “halo” refers to a halogen atom selected from Cl, Br, I, and F.

[0120] The term “alkyl” refers to both straight- and branched-chain moieties. Unless otherwise specifically stated alkyl moieties include between 1 and 6 carbon atoms.

[0121] The term “alkenyl” refers to both straight- and branched-chain moieties containing at least one —C═C—. Unless otherwise specifically stated alkenyl moieties include between 1 and 6 carbon atoms.

[0122] The term “alkoxy” refers to —O-alkyl groups.

[0123] The term “cycloalkyl” refers to a cyclic alkyl moiety. Unless otherwise specifically stated cycloalkyl moieties will include between 3 and 7 carbon atoms.

[0124] The term “amino” refers to —NH₂.

[0125] The term “aryl” refers to phenyl and naphthyl.

[0126] The term “het” refers to mono- or bicyclic ring systems containing at least one heteroatom selected from O, S, and N. Each monocyclic ring may be aromatic, saturated, or partially unsaturated. A bicyclic ring system may include a monocyclic ring containing at least one heteroatom fused with a cycloalkyl or aryl group. A bicyclic ring system may also include a monocyclic ring containing at least one heteroatom fused with another het, monocyclic ring system.

[0127] Examples of “het” include, but are not limited to, pyridine, thiophene, furan, pyrazoline, pyrimidine, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, 3-pyridazinyl, 4-pyridazinyl, 3-pyrazinyl, 4-oxo-2-imidazolyl, 2-imidazolyl, 4-imidazolyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl, 2-oxazolyl, 4-oxazolyl, 4-oxo-2-oxazolyl, 5-oxazolyl, 1,2,3-oxathiazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,2,5-oxadiazole, 1,3,4-oxadiazole, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 3-isothiazole, 4-isothiazole, 5-isothiazole, 2-furanyl, 3-furanyl, 2-thienyl, 3-thienyl, 2-pyrrolyl, 3-pyrrolyl, 3-isopyrrolyl, 4-isopyrrolyl, 5-isopyrrolyl, 1,2,3,-oxathiazole-1-oxide, 1,2,4-oxadiazol-3-yl, 1,2,4-oxadiazol-5-yl, 5-oxo-1,2,4-oxadiazol-3-yl, 1,2,4-thiadiazol-3-yl, 1,2,4-thiadiazol-5-yl, 3-oxo-1,2,4-thiadiazol-5-yl, 1,3,4-thiadiazol-5-yl, 2-oxo-1,3,4-thiadiazol-5-yl, 1,2,4-triazol-3-yl, 1,2,4-triazol-5-yl, 1,2,3,4-tetrazol-5-yl, 5-oxazolyl, 3-isothiazolyl, 4-isothiazolyl, 5-isothiazolyl, 1,3,4,-oxadiazole, 4-oxo-2-thiazolinyl, 5-methyl-1,3,4-thiadiazol-2-yl, thiazoledione, 1,2,3,4-thiatriazole, 1,2,4-dithiazolone, phthalimide, quinolinyl, morpholinyl, benzoxazoyl, diazinyl, triazinyl, quinolinyl, quinoxalinyl, naphthyridinyl, azetidinyl, pyrrolidinyl, hydantoinyl, oxathiolanyl, dioxolanyl, imidazolidinyl, and azabicyclo[2.2. 1]heptyl.

[0128] The term “heterocycle” refers to a fully saturated het, examples of which include, but are not limited to, morpholinyl, thiomorpholinyl, and tertrahydropyranyl.

[0129] Specific R₃ and R₄ substituents include H, F, Cl, Br, CN, NH₂, NO₂, CH₃.

[0130] Specific structures of A include

[0131] Mammal refers to human or animals.

[0132] The compounds of the present invention are generally named according to the IUPAC or CAS nomenclature system. Abbreviations which are well known to one of ordinary skill in the art may be used (e.g. “Ph” for phenyl, “Me” for methyl, “Et” for ethyl, “O” for oxygen atom, “S” for sulfur atom, “N” for nitrogen atom, “h” for hour or hours and “rt” for room temperature) as described in J.Org.Chem., 67-1, 24A, 2002.

[0133] Other abbreviations and definitions used are defined as follows:

[0134] Hunig's base means diisopropylethyl amine;

[0135] HATU means O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexaflourophosphate;

[0136] in vacuo means at reduced pressure;

[0137] EDCI or EDC means 1-ethyl-3-(3-dimethylaminopropyl)carbodimide;

[0138] HOBT means hydroxybenztriazole;

[0139] Fmoc means 9-fluorenylmethoxycarbonyl;

[0140] trisamine resin means tris(2-aminoethyl)amine, polymer-bound.

[0141] The compounds of the present invention can be converted to their salts, where appropriate, according to conventional methods.

[0142] The term “pharmaceutically acceptable salts” refers to acid addition salts useful for administering the compounds of this invention and include hydrochloride, hydrobromide, hydroiodide, sulfate, phosphate, acetate, propionate, lactate, mesylate, maleate, malate, succinate, tartrate, citric acid, 2-hydroxyethyl sulfonate, fumarate and the like. These salts may be in hydrated form.

[0143] The compounds of Formula I of this invention contain a chiral center, such as at C-5 of the isoxazoline ring, and as such there exist two enantiomers or a racemic mixture of both. This invention relates to both the enantiomers, as well as mixtures containing both the isomers. In addition, depending on substituents, additional chiral centers and other isomeric forms may be present in any of A, B, Z or R₁ group, and this invention embraces all possible stereoisomers and geometric forms in these groups.

[0144] The compounds of this invention are useful for treatment of microbial infections in humans and other warm blooded animals, under both parenteral and oral administration.

[0145] The pharmaceutical compositions of this invention may be prepared by combining the compounds of this invention with a solid or liquid pharmaceutically acceptable carrier and, optionally, with pharmaceutically acceptable adjuvants and excipients employing standard and conventional techniques. Solid form compositions include powders, tablets, dispersible granules, capsules, cachets and suppositories. A solid carrier can be at least one substance which may also function as a diluent, flavoring agent, solubilizer, lubricant, suspending agent, binder, tablet disintegrating agent, and encapsulating agent. Inert solid carriers include magnesium carbonate, magnesium stearate, talc, sugar, lactose, pectin, dextrin, starch, gelatin, cellulosic materials, low melting wax, cocoa butter, and the like. Liquid form compositions include solutions, suspensions and emulsions. For example, there may be provided solutions of the compounds of this invention dissolved in water and water-propylene glycol systems, optionally containing suitable conventional coloring agents, flavoring agents, stabilizers and thickening agents.

[0146] Preferably, the pharmaceutical composition is provided employing conventional techniques in unit dosage form containing effective or appropriate amounts of the active component, that is, the compound according to this invention.

[0147] The quantity of active component, that is the compound according to this invention, in the pharmaceutical composition and unit dosage form thereof may be varied or adjusted widely depending upon the particular application, the potency of the particular compound and the desired concentration. Generally, the quantity of active component will range between 0.5% to 90% by weight of the composition.

[0148] In therapeutic use for treating, or combatting, bacterial infections in warm-blooded animals, the compounds or pharmaceutical compositions thereof will be administered orally, parenterally and/or topically at a dosage to obtain and maintain a concentration, that is, an amount, or blood-level of active component in the animal undergoing treatment which will be antibacterially effective. Generally, such antibacterially effective amount of dosage of active component will be in the range of about 0.1 to about 100, more preferably about 1.0 to about 50 mg/kg of body weight/day. It is to be understood that the dosages may vary depending upon the requirements of the patient, the severity of the bacterial infection being treated, and the particular compound being used. Also, it is to be understood that the initial dosage administered may be increased beyond the above upper level in order to rapidly achieve the desired blood-level or the initial dosage may be smaller than the optimum and the daily dosage may be progressively increased during the course of treatment depending on the particular situation. If desired, the daily dose may also be divided into multiple doses for administration, e.g., 2-4 four times per day.

[0149] The compounds according to this invention may be administered parenterally, i.e., by injection, for example, by intravenous injection or by other parenteral routes of administration. Pharmaceutical compositions for parenteral administration will generally contain a pharmaceutically acceptable amount of the compound or a soluble salt (acid addition salt or base salt) dissolved in a pharmaceutically acceptable liquid carrier such as, for example, water-for-injection and a buffer to provide a suitably buffered isotonic solution, for example, having a pH of about 3.5-6. Suitable buffering agents include, for example, trisodium orthophosphate, sodium bicarbonate, sodium citrate, N-methylglucamine, L(+)-lysine and L(+)-arginine to name but a few representative buffering agents. The compound of this invention generally will be dissolved in the carrier in an amount sufficient to provide a pharmaceutically acceptable injectable concentration in the range of about 1 mg/mL to about 400 mg/mL of solution. The resulting liquid pharmaceutical composition will be administered so as to obtain the above-mentioned antibacterially effective amount of dosage. The compounds according to this invention are advantageously administered orally in solid and liquid dosage forms.

[0150] As a topical treatment an effective amount of Formula I is admixed in a pharmaceutically acceptable gel or cream vehicle that can be applied to the patient's skin at the area of treatment. Preparation of such creams and gels is well known in the art and can include penetration enhancers.

[0151] The oxazolidinone antibacterial agents of this invention have useful activity against a variety of organisms. The in vitro activity of compounds of this invention can be assessed by standard testing procedures such as the determination of minimum inhibitory concentration (MIC) by agar dilution as described in “Approved Standard. Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically”, 3rd. ed., published 1993 by the National Committee for Clinical Laboratory Standards, Villanova, Pa., USA.

[0152] Compounds in this invention can be prepared as shown in Schemes I to IV. In Scheme I an amine (1) is condensed with a suitably substituted carboxylic acid (HOOC—CH₂Z′) to give an amide (2) where Z′ represents Z of formula I or a group that can be transformed to Z by subsequent chemistry and where W′ represents W of formula I plus NP where P is a suitable nitrogen protecting group that can be removed at an appropriate time in a manner that is compatible with other substituents on the molecule to give the primary amine (W′═NH₂) which can then be used to prepare compounds where W is NHC(X)R₁ (see the preparation of 7 in Scheme II). A variety of reagents and reaction condensations can be used for the condensations of 1 with the carboxylic acids (HOO—CH₂Z′). These include but are not limited to the carbodiimides such as dicyclohexylcarbodiimide (DCC) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) which can be used with promoters such as 4-(dimethylamino)pyridine (DMAP) or 1-hydroxybenzotriazole (HOBT) in solvents such as DMF or pyridine at 0° C. to 50° C.; and the chloroformates such as isobutyl chloroformate with a tertiary amine such as triethylamine or diisopropylethylamine in solvents such as THF at 0° C. to 25° C.

[0153] Scheme II illustrates the preparation of compounds of formula I where Z is (a). In this scheme, 3 (compound 2 of Scheme I where B″ is (b), Z′ is

[0154] and W′ is NHBoc) is allowed to react with triphenylphosphine and carbon tetrabromide in a solvent such as CH₂Cl₂ at 20° C. to 40° C. to give the bromide (4). Alkylation of primary and secondary amines with 4 can be conveniently carried out in solvents such as MeOH, EtOH and/or acetone at 0° C. to 30° C. Sodium iodide can be used as a catalyst for this reaction. Removal of the tert-butyoxycarbonyl (Boc) protecting group of 5 (R′ and R″=alkyl) to give 6 can be accomplished with an acid catalyst, conveniently 4N HCl in dioxane at 0° C. to 30° C. Acylation of 6 with an activated carboxylic acid derivative such as acetic anhydride in pyridine or propionyl chloride and triethylamine in CH₂Cl₂ will give the corresponding amides (7, X═O). Thioacylation of 6 to give 7 (X═S) can be accomplished by the reactions of 6 with dithioesters and triethylamine in methanol; difluorothioacetamides are conveniently prepared by the reactions of 6 with an ester of difluorothioacetic acid, such as O-(3,3-diphenylpropyl)difluoroethanethioate, in a solvent such as CH₂Cl₂ and/or MeOH. A tertiary amine can be used to neutralize a salt of 6 in this reaction. Compounds of formula 7 where R′ or R″ is hydrogen can best be obtained by protecting the secondary amine (5) in this sequence with an acid stable protecting group. The 9-fluorenylmethyl carbamate (Fmoc) is suitable for this purpose. It can be removed from compound 7 by the reaction with a mild base such as piperidine. Compounds of formula 7 where both R′ and R″ are hydrogen can be obtained by allowing compound 4 to react with sodium azide in DMF. The resulting azide can then be reduced to the amine (5 where R′ and R″ are hydrogen) by hydrogenation with a platinum or palladium catalyst. Fmoc protection of this amine, conversion to the Fmoc protected analogs of 6 and 7 and subsequent deprotection will give the desired compounds of formula 7 (R′═R″═H). Acylation of 5 (where R′ and/or R″ is hydrogen) with Fmoc protected amino acids or dipeptides using for example, conditions described for the preparation of 2 in Scheme I, conversion to the Fmoc protected analogs of 6 and 7 and deprotection will give 7 where R′ or R″ is C(O)CH(R₇)NR₈R₉.

[0155] Scheme III and IV illustrate the preparation of compounds of formula I where Z is (b), (c) or (d). For this type of compound it is often convenient to begin with a preformed side chain. Thus, for example, bromination of 8 with N-bromosuccinimide and light in chloroform gives 9 which is allowed to react with primary or secondary amines (HNR′R″) in acetone to give 10. At this stage secondary amines (R′ or R″═H) can be acylated with activated carboxylic acid or sulfonic acid derivatives or protected with, for example, Boc, Fmoc or benzyloxycarbonyl (Cbz) groups. The ester is then hydrolyzed with an alkali metal hydroxide. It is convenient to use lithium hydroxide in mixtures of MeOH and water at ambient temperature for this reaction and the resulting salt (11) or the corresponding acid can be condensed with 1 as described in Scheme I to obtain 12. Primary amines (12, R′═R″═H) are obtained by allowing 9 to react with sodium azide in DMF. Hydrolysis of the resulting azido ester to the corresponding acid and condensation with 1 gives 13. Reduction of the azide (13) by hydrogenation with a palladium catalyst or other method known in the art will then give 12 (R′═R″═H) which can be converted to other desired compounds of formula I.

[0156] By using the chemistry described in Scheme III and employing other side chains known in the literature or described in the examples other compounds of formula I where Z is (b), (c), or (d) can be prepared. This is further illustrated in Scheme IV where the nitro substituted phthalimide (14), prepared as described in Scheme I, can be reduced by transfer hydrogenation with cyclohexene and a palladium catalyst in refluxing ethanol to give 15. Condensation of 15 with a protected amino acid will then give 16 which can be converted to compounds of formula I as described in Schemes II and III.

[0157] Suitable intermediates useful in preparating compounds of formula I and additional synthetic methods to assist in producing compounds of formula I may be found, for example, in the following publications each of which is hereby incorporated by reference.

[0158] U.S. Pat. Nos. 5,225,565; 5,182,403; 5,164,510; 5,247,090; 5,231,188; 5,565,571; 5,547,950; 5,529,998; 5,627,181; 5,843,967; 5,861,413; 5,827,857; 5,869,659; 5,952,324; 5,968,962; 5,688,792; 6,069,160; 6,239,152; 5,792,765; 4,705,799; 5,043,443; 5,652,238; 5,827,857; 5,529,998; 5,684,023; 5,627,181; 5,698,574; 6,166,056; 6,194,441; 6,110,936; 6,069,145; 6,271,383; 5,981,528; 6,051,716; 6,043,266; 6,313,307; and 5,523,403.

[0159] U.S. patent application Publication 2002/0086900.

[0160] PCT Application and publications PCT/US93/04850, WO94/01110; PCT/US94/08904, WO95/07271; PCT/US95/02972, WO95/25106; PCT/US95/10992, WO96/13502; PCT/US96/05202, WO96/35691; PCT/US96/12766; PCT/US96/13726; PCT/US96/14135; PCT/US96/17120; PCT/US96/19149; PCT/US97/01970; PCT/US95/12751, WO96/15130, PCT/US96/00718, WO96/23788, WO98/54161, WO99/29688, WO99/03846, WO99/37641, WO99/37652, WO99/40094, WO97/30995, WO97/09328, WO01/81350, WO01/40236, WO00/21960 WO01/4022, and WO95/07271.

[0161] In some embodiments, the antibacterial compounds are prodrugs of the compounds of formula I. The expression “prodrug” denotes a derivative of a known direct acting drug, which is transformed into the active drug by an enzymatic or chemical process. Prodrugs of the compounds of formula I are prepared by modifying functional groups present on the compound in such a way that the modifications are cleaved, either in routine manipulation or in vivo, to the parent compound. Prodrugs include, but are not limited to, compounds of structure (I) wherein hydroxy, amine or sulfhydryl groups are bonded to any group that, when administered to the animal, cleaves to form the free hydroxyl, amino or sulfhydryl group, respectively. Representative examples of prodrugs include, but are not limited to, acetate, formate and benzoate derivatives of alcohol and amine functional groups. See Notari, R. E., “Theory and Practice of Prodrug Kinetics,” Methods in Enzymology, 112:309-323 (1985); Bodor, N., “Novel Approaches in Prodrug Design,” Drugs of the Future, 6(3):165-182 (1981); and Bundgaard, H., “Design of Prodrugs: Bioreversible-Derivatives for Various Functional Groups and Chemical Entities,” in Design of Prodrugs (H. Bundgaard, ed.), Elsevier, N.Y. (1985).

EXAMPLES

[0162] Without further elaboration, it is believed that one skilled in the art can, using the preceding description, practice the present invention to its fullest extent. The following detailed examples describe how to prepare the various compounds and/or perform the various processes of the invention and are to be construed as merely illustrative, and not limitations of the preceding disclosure in any way whatsoever. Those skilled in the art will promptly recognize appropriate variations from the procedures both as to reactants and as to reaction conditions and techniques.

Example 1 N-[((5S)-3-{4-[4-({4-[(Diethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide (22)

[0163] Step 1:

[0164] An ice cold, stirred mixture of 17a (15.1 g, 38.3 mmol), 4-(hydroxymethyl)phenoxyacetic acid (6.98 g, 38.3 mmol), 1-hydroxybenzotriazole hydrate (HOBT, 5.69 g, 42.1 mmol) and DMF (195 ml) was treated with 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 14.7 g, 76.6 mmol), allowed to warm slowly to ambient temperature and stand for 18 h. It was then mixed with water (500 ml) and Et₂O (500 ml); the precipitate was collected by filtration, washed carefully with water and then 1:1 heptane: Et₂O and dried to give 19.8 g of 18, an off-white solid. A sample of this material that had been purified by silica gel chromatography with 2.5% MeOH—CH₂Cl₂ and trituration with EtOAc-heptane had: mp 148-154° C.; ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.34 (s, 9H), 2.92, 2.98 (s, s, 4H), 3.25 (m, 2H), 3.60 (s, 4H), 3.73 (dd, 1H), 4.06 (t, 1H), 4.39 (d, 2H), 4.67 (m, 1H), 4.82 (s, 2H), 5.04 (t, 1H), 6.87 (d, 2H), 7.06 (t, 1H), 7.18 (m, 4H), 7.49 (dd, 1H);

[0165] Step, 2:

[0166] A stirred mixture of 18 (3.00 g, 5.37 mmol) and triphenylphosphine (2.16 g, 8.22 mmol) in CH₂Cl₂ (90 ml) was treated with carbon tetrabromide (2.69 g, 8.6 mmol) and kept at ambient temperature for 1 h. Additional triphenylphosphine (216 mg) and carbon tetrabromide (269 mg) were added and the mixture was stirred for 20 min and then concentrated in vacuo. The residue was stirred for 2 h with a mixture of Et₂O (80 ml), heptane (80 ml), and water (60 ml) and then filtered. The solid was washed with water, 1:1 Et₂O: heptane and heptane and dried to give 3.76 g of 19 which was used without further purification: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.34 (s, 9H), 2.93, 2.99 (s, s, 4H), 3.25 (m, 2H), 3.60 (s, 4H), 3.74 (dd, 1H), 4.06 (t, 1H), 4.67 (m, 1H), 4.68 (s, 2H), 4.87 (s, 2H), 6.89 (d, 2H), 7.06 (t, 1H), 7.18 (m, 2H), 7.35 (d, 2H), 7.48 (dd, 1H)

[0167] Step 3:

[0168] A stirred mixture of 19 (2.50 g), diethylamine (1.98 ml, 19.1 mmol), sodium iodide (15 mg) and acetone (98 ml) was kept at ambient temperature for 18 h and mixed with water (50 ml). It was extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated to give 2.44 g of 20, a light brown foam: MS (EI) m/z 613.0 (M⁺), 541.0, 485.5, 441.1, 277.1, 221.5; IR (drift) 3411, 3331, 1746, 1708, 1675 cm⁻¹.

[0169] Step 4:

[0170] Compound 20 (2.44 g) was cooled in an ice bath and treated with 4N HCl in dioxane (30 ml). The mixture was stirred in the ice bath for 1 h and at ambient temperature for 1 h and then concentrated in vacuo. The residue was triturated three times with CH₂Cl₂ (70 ml) with concentration after each addition. A mixture of the resulting material and saturated NaHCO₃ (60 ml) was extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with 10% MeOH-1% NH₄OH—CH₂Cl₂ and crystallization of the product from EtOAc-MeOH-heptane gave 1.01 g of 21: mp 98° C. with softening and foaming from 92° C.; ¹H NMR [300 MHz, (CD₃)₂SO] δ 0.93 (t, 6H), 2.02 (broad s), 2.39 (q, 4H), 2.79 (m, 2H), 2.92, 2.98 (s, s, 4H), 3.42 (s, 2H), 3.60 (s, 4H), 3.80 (dd, 1H), 4.01 (t, 1H), 4.58 (m, 1H), 4.81 (s, 2H); 6.85 (d, 2H), 7.05 (t, 1H), 7.18 (m, 3H), 7.50 (dd, 1H),; MS (EI) m/z 513.0 (M⁺), 498.2, 484.1, 441.2, 412.1, 350.0, 335.3, 293.6.

[0171] Step 5:

[0172] A stirred mixture of 21 (300 mg, 0.584 mmol), triethylamine (204 μL, 1.46 mmol) and MeOH (6.5 ml) was treated with ethyl dithiopropionate (94 mg, 0.701 mmol) and kept at ambient temperature for 18 h. It was then diluted with CH₂Cl₂, mixed with silica gel (2.5 g) and concentrated in vacuo. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄OH—CH₂Cl₂ and crystallization of the product from EtOAc-heptane-Et₂O gave 155 mg of 22, an off white solid: ¹H NMR [300 MHz, (CD₃)₂SO] δ 0.94 (t, 6H), 1.22 (t, 3H), 2.39 (m, 4H), 2.56 (q, 2H), 2.92, 2.99 (s, , 4H), 3.42 (s, 2H), 3.60 (s, 4H), 3.78 (dd, 1H), 3.90 (t, 2H), 4.11 (t, 1H), 4.82 (s, 2H), 4.93 (m, 1H), 6.85 (d, 2H), 7.06 (t, 1H), 7.16 (m, 3H), 7.49 (dd, 1H), 10.32 (s, 1H).

Example 2 N-[((5S)-3-{4-[4-({4-[(Diethylamnino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]cyclopropanecarbothioamide (23)

[0173]

[0174] As described for the preparation of 22, the reaction of 7 (300 mg, 0.584 mmol) with ethyl cyclopropanecarbodithioate gave 146 mg of 23; ¹HNMR [300 MHz, (CD₃)₂SO] δ 0.94 (m, 10H), 2.14 (m, 1H), 2.39 (m, 4H), 2.93, 2.99 (s, s, 4H), 3.42 (s, 2H), 3.61 (s, 4H), 3.79 (dd, 1H), 3.94 (m, 2H), 4.12 (t, 1H), 4.82 (s, 2H), 4.93 (m, 1H), 6.85 (d, 2H), 7.06 (t, 1H), 7.18 (m, 3H), 7.50 (dd, 1H), 10.52 (t, 1H); MS (EI) m/z 597.2 (M⁺), 553.4, 524.4, 247.7.

Example 3 N-[((5S)-3-{4-[4-({4-[(Diethylamnino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide (24)

[0175]

[0176] A stirred mixture of 21 (300 mg, 0.584 mmol), triethylamine (0.65 ml, 4.7 mmol), THF (5.8 ml) and CH₂Cl₂ (5.8 ml) was treated with acetyl chloride (76 μL, 0.88 mmol) and kept at ambient temperature for 18 h. It was then diluted with CH₂Cl₂, mixed with silica gel (2.5 g) and concentrated. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄OH—CH₂Cl₂ and crystallization of the product from EtOAc-heptane-Et₂O gave 122 mg of 24, a white solid: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.17 (m, 6H), 1.81 (s, 3H), 3.02 (m, 8H), 3.38 (t, 2H), 3.60 (s, 4H), 3.70 (dd, 1H), 4.07 (t, 1H), 4.19 (d, 2H), 4.79 (m, 1H), 4.91 (s, 2H), 6.98 (d, 2H), 7.06 (t, 1H), 7.16 (dd, 1H), 7.48 (m, 3H), 8.26 (t, 1H).

Example 4 N-[((5S)-3{4-[4-({4-[(Dimethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide (27)

[0177]

[0178] A stirred mixture of 19 (1.88 g), 2M dimethylamine in MeOH (5.1 ml, 10.2 mmol), sodium iodide (36 mg) and acetone (66 ml) was kept at ambient temperature for 20 min and concentrated in vacuo. A mixture of the residue and 1N HCl was washed with Et₂O and EtOAc, cooled in an ice bath and made alkaline with solid NaHCO₃. This was extracted with CH₂Cl₂ and the extract was concentrated. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄OH—CH₂Cl₂ gave 979 mg of 25 that was used without further purification in subsequent reactions: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.33 (s, 9H), 2.14 (s, 6H), 2.92, 2.98 (s, s, 4H), 3.24 (t, 2H), 3.36 (s, 2H), 3.60 (s, 4H), 3.74 (dd, 1H), 4.06 (t, 1H), 4.66 (m, 1H), 4.83 (s, 2H), 6.87 (d, 2H), 7.05 (t, 1H), 7.16 (m, 4H), 7.48 (dd, 1H); MS (EZ) m/z 585.1 (M+), 541.3, 528.2, 512.2, 485.2, 470.2, 277.2, 262.5.

[0179] Step 2:

[0180] Solid 25 (357 mg) was cooled in an ice bath and treated with 4N HCl in dioxane (10 ml). The stirred mixture was kept in the ice bath for 1 h and at ambient temperature for 1 h and then concentrated in vacuo. The residue was triturated three times with 50 ml portions of CH₂Cl₂, concentrating the mixture after each addition, to give 26, a white solid: MS (EI) m/z 485.2 (M⁺), 470.3, 442.4, 335.7, 293.6, 261.6; IR(drift) 3330, 1757, 1662, 1627 cm⁻¹.

[0181] Step 3:

[0182] A stirred mixture of 26 (prepared from 357 mg of 25), triethylamine (0.68 ml, 4.88 mmol) and MeOH (8.5 ml) was treated with methyl dithiopropionate⁴ (293 mg, 2.44 mmol), and kept at ambient temperature for 3 h. It was then concentrated in vacuo. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄OH—CH ₂Cl₂ and crystallization of the product from EtOAc gave 204 mg of 13 a white solid: mp 163-164° C.; ¹HNMR [300 MHz, (CD₃)₂SO] δ 1.12 (t, 3H), 2.09 (s, 6H), 2.56 (q, 2H), 2.92, 2.99 (s, s, 4H), 3.28 (s, 2H), 3.60 (s, 4H), 3.78 (dd, 1H), 3.90 (t, 2H), 4.11 (t, 1H), 4.82 (s, 2H), 4.93 (m, 1H), 6.86 (d, 2H), 7.06 (t, 1H), 7.15 (m, 3H), 7.49 (dd, 1H), 10.30 (t, 1H); MS (EI) m/z 557.1 (M⁺), 513.1, 354.1, 165.4; MS (CD) m/z 558.1 (M+H⁺); IR (drift) 3235, 1750, 1653 cm⁻¹. Anal. calcd for C₂₈H₃₆FN₅O₄S: C, 60.30; H, 6.51; N, 12.56. Found: C, 60.08; H, 6.47; N, 12.44 cm⁻¹.

Example 5 N-[((5S)-3-{4-[4-({4-[(Dimethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]cyclopropanecarbothioamide (28)

[0183]

[0184] As described for the preparation of 27, the reaction of 26 (prepared from 357 mg of 25) with ethyl cyclopropanecarbodithioate and triethylamine gave the thioamide which was mixed with saturated NaHCO₃ and extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄OH—CH₂Cl₂ and crystallization of the product from Et₂O—CH₂Cl₂-heptane gave 74 mg of 28: mp 169-170° C.; ¹H NMR [300 MHz, (CD₃)₂SO] δ 0.84 (m, 2H), 1.01 (m, 2H), 2.12 (s, 7H), 2.93. 3.00 (s, s, 4H), 3.25 (s, 2H), 3.60 (s, 4H), 3.79 (dd, 1H), 3.94 (m, 2H), 4.12 (t, 1H), 4.83 (s, 2H), 4.92 (m, 1H), 6.86 (d, 2H), 7.07 (t, 1H), 7.17 (m, 3H), 7.49 (dd, 1H).

Example 6 N-[((5S)-3-{4-[4-({4-[(Dimethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide (29)

[0185]

[0186] As described for the preparation of 27, the reaction of 26 (prepared from 264 mg of 25) with acetyl chloride and triethylamine gave the acetamide which was purified by silica gel chromatography with 5% MeOH-0.5%NH₄OH—CH₂Cl₂ followed by crystallization from Et₂OAc to give 73 mg of 29, a white solid; ¹HNMR [300 MHz, (CD₃)₂SO] δ 1.81 (s, 3H), 2.45 (s, 6H), 2.93. 3.00 (s, s, 4H), 3.38 (t, 2H), 3.60 (s, 4H), 3.68 (dd, 1H), 3.85 (s, 2H), 4.06 (t, 1H), 4.69 (m, 1H), 4.88 (s, 2H), 6.94 (d, 2H), 7.06 (t, 1H), 7.16 (dd, 1H), 7.33 (d, 2H), 7.49 (dd, 1H), 8.24 (t, 1H).

Example 7 N-({(5S)-3-[3-Fluoro-4-(4-{[4-(morpholin-4-ylmethyl)phenoxy]acetyl}piperazin-1-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)propanethioamide (32)

[0187] Step 1:

[0188] A stirred mixture of 19 (1.88 g), morpholine (1.1 ml, 12.8 mmol) sodium iodide (36 mg) and acetone (29 ml) was kept at ambient temperature for 18 h and concentrated in vacuo. A mixture of the residue in 1N HCl (15 ml) was washed with Et₂O and EtOAc, cooled in an ice bath and made alkaline with solid NaHCO₃. It was extracted with CH₂Cl₂ and the extract was concentrated. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄OH—CH₂Cl₂ gave 773 mg of 30. Rechromatography of the impure fractions with 2.5% MeOH-0.25% NH₄OH—CH₂Cl₂ and trituration of the product with EtOAc-heptane gave 280 mg of additional 15: mp 166-168° C.; ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.33 (s, 9H), 2.29 (s, 4H), 2.92, 2,98 (s, s, 4H), 3.24 (t, 2H), 3.35 (s, 2H), 3.53 (t, 4H), 3.60 (s, 4H), 3.74 (dd, 1H), 4.06 (t, 1H), 4.66 (m, 1H), 4.82 (s, 2H), 6.86 (d, 2H), 7.05 (t, 1H), 7.19 (m, 4H), 7.48 (dd, 1H).

[0189] Step 2:

[0190] As described for the preparation of 26 the reaction of 30 (770 mg, 1.23 mmol) with 4N HCl in dioxane gave 31: MS (EI) m/z 527.2 (M⁺), 441.5, 334.4; IR (drift) 3330, 1758, 1666, 1626 cm⁻¹.

[0191] Step 3:

[0192] As described for the preparation of 27, the reaction of 31 (prepared from 385 mg of 30) with methyl dithiopropionate and crystallization of the product from EtOAc-heptane gave 308 mg of 32: mp 159-160° C.; ¹HNMR [300 MHz, (CD₃)₂SO] δ 1.12 (t, 3H), 2.29 (s, 4H), 2.56 (q, 2H), 2.92, 2.99 (s, s, 4H), 3.35 (s, 2H), 3.53 (t,4H), 3.60 (s, 4H), 3.78 (dd, 1H), 3.90 (t, 2H), 4.11 (t, 1H), 4.82 (s, 2H), 4.93 (m, 1H), 6.86 (d, 2H), 7.06 (t, 1H), 7.17 (m, 3H), 7.49 (dd, 1H), 10.30 (t, 1H); MS (FAB) m/z 600 (M+H⁺), 599.4, 513.3; HRMS calcd for C₃₀H₃₉FN₅O₅S (M+H⁺), 600.2656, found 600.2666; IR (drift) 3306, 3236, 1749, 1653 cm⁻¹. Anal. calcd for C₃₀H₃₈FN₅O₅S: C, 60.08; H, 6.39; N, 11.68. Found: C, 59.60; H, 6.47; N, 11.56.

Example 8 N-({(5S)-3-[3-Fluoro-4-(4-{[4-(morpholin-4-ylmethyl)phenoxy]acetyl}piperazin-1-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)cyclopropanecarbothioamide (33)

[0193]

[0194] As described for the preparation of 27, the reaction of 31 (prepared from 385 mg of 25) with ethyl cyclopropanecarbodithioate and crystallization of the product from EtOAc-heptane gave 290 mg of 33: mp 138-141° C.; ¹H NMR[300 MHz, (CD₃)₂SO] δ 0.84 (m, 2H), 1.01 (m, 2H), 2.14 (m, 1H), 2.29 (s, 4H), 2.93, 2.99 (s, s, 4H), 3.35 (s, 2H), 3.53 (t, 4H), 3.60 (s, 4H), 3.78 (dd, 1H), 3.94 (m, 2H), 4.12 (t, 1H), 4.82 (s, 2H), 4.93 (m, 1H), 6.86 (d, 2H), 7.06 (t, 1H), 7.17 (m, 3H), 7.50 (dd, 1H), 10.50 (t, 1H);

Example 9 N-({(5S)-3-[3-]Fluoro-4-(4-{[4-(morpholin-4-ylmethyl)phenoxy]acetyl(piperazin-1-yl)phenyl]-2-oxo-1,3-oazolidin-5-yl]methyl)acetamide (34)

[0195]

[0196] As described for the preparation of 24, the reaction of 31 (prepared from 260 mg of 30) with acetyl chloride and triethylamine and crystallization of the product from EtOAc-heptane gave 194 mg of 34, a white solid; mp 143-147° C.; ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.81 (s, 3H), 2.29 (s, 4H), 2.92, 2.99 (s, s, 4H), 3.36 (s, 2H), 3.38 (t, 2H), 3.53 (s, 4H), 3.60 (s, 4H), 3.68 (dd, 1H), 4.06 (t, 1H), 4.69 (m, 1H), 4.82 (s, 2H), 6.86 (d, 2H), 7.05 (t, 1H), 7.17 (m, 3H), 7.48 (dd, 1H), 8.23 (t, 1H).

Example 10 N-[((5S)-3-{3-Fluoro-4-[4-({4-[(4-methylpiperazin-1-yl)methyl]phenoxy}acetyl)piperazin-1-yl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide (37)

[0197] Step 1:

[0198] A stirred mixture of 19 (2.50 g), N-methyl-piperazine (2.10 ml, 19.1 mmol), acetone (98 ml) and a small amount of NaI was kept at ambient temperature for 18 h and concentrated in vacuo. A solution of the residue in 1N HCl (20 ml) was washed with EtOAc and then Et₂O (emulsions which were difficult to separate were formed in this process). The aqueous layer was adjusted to pH 10 with solid NaHCO₃ and extracted with CH₂Cl₂. The extract was concentrated to give 1.67 g of 35, a brown foam: MS (EI) m/z 640.1 (M⁺), 611.0, 582.0, 540.0, 394.1, 262.5; HRMS calcd for C₃₃H₄₆FN₆O₆ (M+H⁺) 641.3463, found 641.3455.

[0199] Step 2:

[0200] Compound 35 (1.67 g) was cooled in an ice bath and treated with 4N HCl in dioxane (20 ml). The stirred mixture was kept in the ice bath for 1 h and at ambient temperature for 1 h and concentrated in vacuo. The residue was triturated with three portions of CH₂Cl₂ (50 ml) with concentration after each addition. A mixture of the solid residue and saturated NaHCO₃ (50 ml) was extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with 10% MeOH-1% NH₄OH—CH₂Cl₂ and crystallization of the product from EtOAc-CH₂Cl₂-heptane gave 389 mg, mp 134-135° C. which contained a small amount of less polar impurity by TLC, and 567 mg, mp 138-141° C. of pure 36: MS (EI) m/z 540.0 (M⁺), 511.0, 469.1, 454.3, 441.1, 350.1; IR (drift) 3325, 3313, 1730, 1664 cm⁻¹.

[0201] Step 3:

[0202] A stirred mixture of 36 (300 mg, 0.555 mmol), triethylamine (193 μL, 1.39 mmol), ethyl dithiopropionate (89 mg, 0.67 mmol) and MeOH (6 ml) was kept at ambient temperature for 18 h, treated with silica gel (2.5 g) and concentrated in vacuo. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄OH—CH₂Cl₂ and crystallization of the product from Et₂O—CH₂Cl₂ gave 175 mg of 37, a white solid: mp 139-144° C. (dec); ¹H NMR [300 MHz, (CD₃SO] δ 1.15 (t, 3H), 2.18 (s, 3H), 2.35 (broad s, 8H), 2.58 (q, 2H), 2.95, 3.00 (s, s, 4H), 3.38 (s, 2H), 3.62 (s, 4H), 3.81 (dd, 1H), 3.92 (t, 2H), 4.13 (t, 1H), 4.84 (s, 2H), 4.95 (m, 1H), 6.88 (d, 2H), 7.08 (t, 1H), 7.18 (m, 3H), 7.51 (dd, 1H), 10.35 (s, 1H).

Example 11 N-[((5S)-3-{3-]Fluoro-4-[4-({4-[(4-methylpiperazin-1-yl)methyl]phenoxy}acetyl)piperazin-1-yl]phenyl)-2-oxo-1,3-oxazolidin-5-yl)methyl]cyclopropanecarbothioamide (38)

[0203]

[0204] Compound 38 was prepared by the reaction of 36 (250 mg, 0.462 mmol) with ethyl cyclopropanecarbodithioate as described for the preparation of 37. Crystallization of the product from Et₂O—CH₂Cl₂ gave a solid which was mixed with saturated NaHCO₃, extracted with CH₂Cl₂: MeOH (9:1) and crystallized: IR (drift) 3302, 1739, 1638 cm⁻¹; MS (Cl) m/z 625.2 (M+H⁺), 581.2; HRMS (FAB) calcd for C₃₂H₄₂FN₆O₄S (M+H⁺) 625.2972, found 625.2961.

Example 12 N-[((5S)-3-{3-Fluoro-4-[4-({4-[(4-methylpiperazin-1-yl)methyl]phenoxy}acetyl)piperazin-1-yl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide (39)

[0205]

[0206] A stirred solution of 36 (250 mg, 0.462 mmol), triethylamine (515 μL, 3.70 mmol), CH₂Cl₂ (4.6 ml) and THF (4.6 mmol) was treated with acetyl chloride (60 μL, 0.69 mmol), kept at ambient temperature for 18 h, treated with silica gel (2.5 g) and concentrated in vacuo. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄H—CH₂Cl₂ gave the product which was crystallized from Et₂O—CH₂Cl₂. The resulting material appeared to be a salt. It was mixed with saturated NaHCO₃ and extracted with 9:1 CH₂Cl₂: MeOH. The extract was dried (MgSO₄) and concentrated. Crystallization of the residue from EtOAc gave 39: IR (drift) 3317, 1726, 1668, 1645 cm⁻¹; MS (EI) m/z 582.3 (M⁺), 538.3, 524.2, 511.2, 467.2, 439.2, 336.2, 294.1; HRMS (FAB) calcd for C₃₀H₄₀FN₆O₅ (M+H⁺) 583.3044, found 583.3045.

Example 13 N-[((5S)-3-{4-[4-(4-{4-[(Dimethylamino)methyl]phenyl}-4-oxobutanoyl)-1-piperazinyl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide (47)

[0207] Step 1:

[0208] A stirred mixture of 4-(4-methylphenyl)-4-oxobutanoic acid (5.00 g, 26.0 mmol) and potassium carbonate (10.8 g, 78.0 mmol) in DMF (50 ml) was treated with methyl iodide (8.1 ml, 130 mmol) and kept at ambient temperature for 3 h. It was then mixed with water (300 ml) and extracted with Et₂O. The extract was washed with water, dried (MgSO₄) and concentrated to give 5.09 g of a light yellow solid (40): mp 40-42° C.; ¹H NMR (300 MHz, CDCl₃) δ 2.41 (s, 3H), 2.75 (t, 2H), 3.30 (t, 2H), 3.70 (s, 3H), 7.26 (d, 2H), 7.88 (d, 2H); MS (EST) m/z 229 (M+Na⁺); IR (drift) 1733, 1679 cm⁻¹.

[0209] Step 2:

[0210] A stirred mixture of 40 (22.0 g, 107 mmol), N-bromosuccinimide (23.7 g, 133 mmol) and CHCl₃ (1600 ml) was kept under a bright (movie) light for 2 h; the mixture refluxed gently. Additional NBS (2.3 g) was added and stirring under the light was continued for 2 h. This mixture was concentrated in vacuo and the residue was stirred for three days with Et₂O (1 L) and then filtered. The solid was washed well with Et₂O and the filtrate was washed with water, dried (MgSO₄) and concentrated. The residue was triturated with 1:1 Et₂O-heptane at ambient temperature for 30 min and at 0° C. for 30 min and then filtered to give 22.5 g of an off-white solid that by NMR was an 85:15 mixture of 41 and 42: ¹H NMR (300 MHz, CDCl₃ for 4) δ 2.77 (t, 2H), 3.31 (t, 2H), 3.71 (s, 3H), 4.50 (s, 2H), 7.49 (d, 2H), 7.96 (d, 2H); ¹H NMR (300 MHz, CDCl₃ for 5) δ 2.78 (t, 2H), 3.31 (t, 2H), 3.71 (s, 3H), 6.65 (s, 1H), 7.66 (d, 2H) A sample of this mixture was purified by silica gel chromatography with 25% EtOAc-heptane to give a sample of 41 with 99.6% purity: mp 163-164° C.; IR (drift) 1729, 1680 cm⁻¹; MS (ESI) m/z 284, 286 (M⁺); HRMS calcd for C₁₂H₁₄BrO₃ (M+H⁺) 285.0127, found 285.0132.

[0211] Step 3:

[0212] A stirred mixture of an 86:14 mixture of 41 and 42 (200 mg), 2 M dimethylamine in MeOH (1.4 ml) and sodium iodide (7 mg) in acetone (9 ml) was kept at ambient temperature for 18 h and concentrated in vacuo. A solution of the residue in 1N hydrochloric acid (5 ml) was washed with Et₂O, made alkaline with 2N NaOH and extracted with Et₂O. The extract was dried (MgSO₄) and concentrated to give 124 mg of 43 which was purified by silica gel chromatography with 5% MeOH—CH₂Cl₂: ¹H NMR (300 MHz, CDCl₃) δ 2.24 (s, 6H), 2.76 (t, 2H), 3.32 (t, 2H), 3.47 (s, 2H), 3.70 (s, 3H), 7.41 (d, 2H), 7.94 (d, 2H).

[0213] Step 4:

[0214] A stirred solution of 43 (632 mg, 2.53 mmol) in MeOH (17 ml) was treated with 1 M LiOH (3.3 ml) and kept at ambient temperature for 5 h. Additional LiOH (1.0 ml) was added and the mixture was kept at ambient temperature for 18 h and concentrated in vacuo. The residue was triturated with Et₂O, filtered, washed with Et₂O and dried to give 732 mg of 44, an off-white solid: mp 198-199° C.; MS (EI) m/z 234.8 (M−Li+H⁺); MS (CI) m/z 236.3 (M−Li+2H⁺), IR (drift) 1679 cm⁻¹.

[0215] Step 5

[0216] A stirred, ice cold mixture of 44 (2.5 mmol), 17a (986 mg, 2.50 mmol), triethylamine (1.05 ml, 7.50 mmol) and hydroxybenzotriazole hydrate (HOBT) (372 mg, 2.75 mmol) in DMF (22 ml) was treated with 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) (1.05 g, 5.50 mmol), warmed to ambient temperature and kept for 18 h. It was then mixed with water (100 ml) and Et₂O (75 ml). A solid precipitated. The Et₂O layer and solid was washed with water; the solid was collected by filtration, washed with Et₂O and dried to give 1.25 g of 45: mp 160-164° C.; 1H NMR [300 MHz, (CD₃)₂SO] δ 1.34 (s, 9H), 2.14 (s, 6H), 2.73 (t, 2H), 2.90, 3.01 (s, s, 4H), 3.22 (m, 4H), 3.44 (s, 2H), 3.58, 3.65 (s, s, 4H), 3.74 (dd, 1H), 4.07 (t, 1H), 4.66 (m, 1H), 7.08 (t, 1H), 7.19 (m, 2H), 7.42 (d, 2H), 7.49 (dd, 1H), 7.93 (d, 2H).

[0217] Step 6:

[0218] A flask containing 45 (1.20 g, 1.96 mmol) was cooled in an ice bath and treated with 4N hydrogen chloride in dioxane (10 ml). The mixture was stirred in the ice bath for 2 h and at ambient temperature for 1.5 h and then concentrated in vacuo. The residue was triturated with three 40 ml portions of CH₂Cl₂ with concentration after each addition to give 46, a white solid: mp>210° C.; MS (EI) m/z 511.2 (M⁺); IR (drift) 3352, 1759, 1685, 1645, 1629 cm⁻¹.

[0219] Step 7:

[0220] A stirred mixture of 46 (0.98 mmol), triethylamine (1.1 ml, 7.84 mmol), methyl dithiopropionate (471 mg, 3.92 mmol) and MeOH (13.6 ml) was kept at ambient temperature for 3 d and concentrated. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄OH—CH₂Cl₂ and crystallization of the product from EtOAc gave 360 mg of 47, a white solid: mp 169° C.; ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.13 (t, 3H), 2.14 (s, 6H), 2.57 (q, 2H), 2.73 (t, 2H), 2.90, 3.00 (s, s, 4H), 3.22 (t, 2H), 3.45 (s, 2H), 3.58, 3.66 (s, s, 4H), 3.80 (d, d, 1H), 3.90 (t, 2H), 4.12 (t, 1H), 4.93 (m, 1H), 7.07 (t, 1H), 7.16 (dd, 1H), 7.42 (d, 2H), 7.48 (dd, 1H), 7.93 (d, 2H), 10.30 (t, 1H),;

Example 14 N-[((5S)-3-{4-[4-(4-{4-[(Dimethylamino)methyl]phenyl}-4-oxobutanoyl)-1-piperazinyl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]cyclopropanecarbothioamide (48)

[0221]

[0222] A stirred mixture of 46 (0.98 mmol), triethylamine (1.1 ml, 7.8 mmol) and MeOH (13.6 ml) was treated with ethyl cyclopropanecarbodithioate (573 mg, 3.92 mmol), kept at ambient temperature for 3 days and concentrated. The residue was chromatographed on silica gel and the product was crystallized from EtOAc to give 375 mg of 48, a white solid: mp 174-175° C.; ¹H NMR [300 MHz, (CD₃)₂SO] δ 0.84 (m, 2H), 1.02 (m, 2H), 2.14 (s, 6H), 2.14 (m, 1H), 2.73 (t, 2H), 2.90, 3.00 (s, s, 4H), 3.22 (t, 2H), 3.45 (s, 2H), 3.58, 3.66 (s, s, 4H), 3.79 (dd, 1H), 3.94 (m, 2H), 4.12 (t, 1H), 4.93 (m, 1H), 7.07 (t, 1H), 7.18 (dd, 1H), 7.43 (d, 2H), 7.50 (dd, 1H), 7.93 (d, 2H), 10.47 (s, 1H); MS (CI) m/z 596 (M+H⁺), 551.2, 536.1, 509.1, 218.1, 174.8, 161.2, 58.1.

Example 15 N-[((5S)-3-{4-[4-(4-{4-[(Dimethylamino)methyl]phenyl}-4-oxobutanoyl)-1-piperazinyl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide (49)

[0223]

[0224] A stirred mixture of 46 (0.981 mmol ), CH₂Cl₂ (10 ml), THF (10 ml) and triethylamine (1.1 ml, 7.85 mmol) was treated with acetyl chloride (128 μL, 1.47 mmol), kept at ambient temperature for 3 days and concentrated in vacuo. The residue was mixed with water and extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄OH—CH₂Cl₂ and crystallization of the product from EtOAc gave 369 mg of 49, and off-white solid: mp 190-192° C.; MS (EI) m/z 553.2 (M⁺), 509.2, 467.4, 334.3, 218.2, 134.1, 84.1, 58.5; IR (drift) 3315, 1743, 1686, 1647 cm⁻¹. Anal. calcd for C₂₉H₃₆FN₅O₅: C, 62.91; H, 6.55; N, 12.65. Found: C, 62.60; H, 6.59; N, 12.59.

Example 16 N-({(5S)-3-[3-Fluoro-4-(4-{4-[4-(4-morpholinylmethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)propanethioamide (54)

[0225] Step 1:

[0226] A stirred mixture of 41 (4.00 g of an 84:16 mixture of 41 and 42, 11.8 mmol of 41), morpholine (4.1 ml, 47 mmol), acetone 180 ml and a small amount of Nal was kept at ambient temperature for 18 h and concentrated in vacuo. A solution of the residue in 1N HCl was washed with Et₂O, adjusted to pH 9-10 with solid NaHCO₃ and extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated to give 3.50 g of 50, a yellow solid: mp 79-80.5° C.; MS (EI) m/z 290.6 (M⁺), 260.1, 218.2, 204.7, 174.6, 89.4, 86.9; IR (drift) 1732, 1684 cm⁻¹.

[0227] Step 2:

[0228] A stirred solution of 50 (3.44 g, 11.8 mmol) in MeOH (80 ml) was treated with 1N LiOH (15 ml), kept at ambient temperature for 18 h and concentrated in vacuo. Two 100 ml portions of Et₂O were added to the residue with concentration after each addition to give 51, a light brown solid: MS (EI) m/z 260.6, 218.8, 204.4, 174.6, 90.3, 57.1; IR (drift) 1668 cm⁻.

[0229] Step 3:

[0230] A stirred, ice cold mixture of 51 (11.8 mmol), 17a (4.42 g, 11.2 mmol), HOBT (1.75 g, 13.0 mmol) and DMF (75 ml) was treated with EDC (4.98 g, 26.0 mmol), allowed to warm slowly to ambient temperature and stand for 3 d. It was then mixed with water (300 ml) and Et₂O (500 ml), a solid formed. The Et₂O-solid mixture was washed with water and filtered. The solid was washed with Et₂O and dried to give 5.72 g of 52, an off-white solid: mp 128-131° C.; MS (FAB) m/z 654.3 (M+H⁺), 598.3, 393.2, 260.1, 100.1, 57.1; HRMS (FAB) calcd for C₃₄H₄₅FN₅O₇ (M+H⁺) 654.3303, found 654.3289; IR (drift) 1742, 1710, 1687, 1652 cm⁻¹.

[0231] Step 4:

[0232] Solid 52 (4.00 g, 6.29 mmol) was cooled in an ice bath and treated with 4NHCl in dioxane (40 ml). The stirred mixture was kept in the ice bath for 1 h and at ambient temperature for 1 h and then concentrated in vacuo. Three 50 ml portions of CH₂Cl₂ were added to the residue with concentration after each addition to give 53, an off-white solid: MS (EI) m/z 553.0 (M⁺), 467.2, 454.1, 377.4, 292.2, 259.3, 174.6, 86.4; IR (drift) 1759, 1685, 1646, 1627, 1608 cm⁻¹.

[0233] Step 5:

[0234] A stirred solution of 49 (one third of the product from the previous reaction—about 2.07 mmol) and triethylamine (2.31 ml, 16.6 mmol) in MeOH (28 ml) was treated with methyl dithiopropionate⁵ (996 mg, 8.28 mmol) and kept at ambient temperature for 18 h. It was then concentrated in vacuo. The residue was mixed with saturated NaHCO₃ and extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with 2.5% MeOH-0.25% NH₄OH—CH₂Cl₂ and crystallization of the product first from EtOAc and then EtOH gave 727 mg of 50: mp 160° C.; ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.13 (t, 3H), 2.35 (s, 4H), 2.57 (q, 2H), 2.73 (m, 2H), 2.90, 3.00 (s, s, 4H), 3.22 (m, 2H), 3.55 (m, 8H), 3.66 (s, 2H), 3.79 (m, 1H), 3.90 (m, 2H), 4.12 (t, 1H), 4.93 (m, 1H), 7.07 (t, 1H), 7.16 (d, 1H), 7.46 (m, 3H), 7.93 (d, 2H), 10.31 (s, 1H); MS (FAB) m/z 626.3 (M+H⁺), 260.2, 204.2, 100.1, 86.1; IR (drift) 3250, 1743, 1683, 1647 cm⁻¹. Anal. calcd for C₃₂H₄₀FN₅O₅S: C, 61.42; H, 6.44; N, 11.19. Found: C, 61.26; H, 6.48; N, 11.12.

Example 17 N-({(5S)-3-[3-Fluoro-4-(4-{4-[4-(4-morpholinylmethyl)phenyl]-4--oxobutanoyl}-1-piperazinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide (55)

[0235]

[0236] A stirred mixture of 53 (about 2.07 mmol), triethylamine (2.3 ml, 16.6 mmol), CH₂Cl₂ (21 ml) and THF (21 ml) was treated with acetyl chloride (270 mg, 3.11 mmol) and kept at ambient temperature for 18 h. It was concentrated in vacuo and the residue was mixed with saturated NaHCO₃ and extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with mixtures of MeOH—NH₄OH—CH₂Cl₂ containing 2.5-10% MeOH and 0.25-1% NH₄OH gave the product which was crystallized from EtOH to give 835 mg of 55: mp 178-179° C.; ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.82 (s, 3H), 2.34 (m, 4H), 2.73 (t, 2H), 2.90 3.00 (s, s, 4H), 3.22 (t, 2H), 3.39 (t, 2H), 3.55 (m, 8H), 3.66 (m, 3H), 4.07 (t, 1H), 4.69 (m, 1H), 7.07 (t, 1H), 7.17 (dd, 1H), 7.46 (m, 3H), 7.93 (d, 2H), 8.21 (t, 1H),

Example 18 N-({(5S)-3-[3-Fluoro-4-(4-{4-[4-(4-morpholinylmethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)cyclopropanecarbothioamide (56)

[0237]

[0238] A stirred solution of 53 (about 2.07 mmol) and triethylamine (2.3 ml, 16.6 mmol) in MeOH (28 ml) was treated with ethyl cyclopropanecarbodithioate (1.21 g, 8.28 mmol), kept at ambient temperature for 18 h and concentrated in vacuo. A mixture of the residue in saturated NaHCO₃ was extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with 2.5% MeOH-0.25% NH₄OH—CH₂Cl₂ and crystallization of the product first from EtOAc and then from EtOH gave 713 mg of 56: mp 173-174° C.; ¹H NMR [300 MHz, (CD₃)₂SO] δ 0.84 (m, 2H), 1.02 (m, 2H), 2.15 (m, 1H), 2.35 (m, 4H), 2.73 (t, 2H), 2.90, 3.00 (s, s, 4H), 3.22 (t, 2H), 3.55 (m, 8H), 3.66 (s, 2H), 3.79 (dd, 1H), 3.94 (m, 2H), 4.12 (t, 1H), 4.93 (m, 1H), 7.07 (t, 1H), 7.18 (dd, 1H), 7.44 (d, 2H), 7.50 (dd, 1H), 7.93 (d, 2H), 10.47 (s, 1H).

Example 19 N-[((5S)-3-{3-Fluoro-4-[4-(4-{4-[(methylamino)methyl]phenyl}-4-oxobutanoyl)piperazin-1-yl]phenyl]-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide (60)

[0239] Step 1:

[0240] a) A solution of 4 (1.00 g of an 85:15 mixture of 4 and 5) in THF (10 ml) was added to a stirred 2M solution of methylamine in THF (35 ml), kept at ambient temperature for 1 h and concentrated in vacuo. A solution of the residue in dilute HCl (10 ml) was washed with Et₂O and then made alkaline with solid NaHCO₃.

[0241] b) The mixture of step a) was treated with THF (25 ml), cooled in an ice bath and with stirring, treated with di-(tert-butyl)dicarbonate (998 mg, 4.58 mmol). It was allowed to warm slowly to ambient temperature and stand for 4 h. It was then extracted with Et₂O. The extract was dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with 25% EtOAc-heptane gave 816 mg of 57: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.35, 1.42 (s, s, 9H), 2.63 (t, 2H), 2.77 (s, 3H), 3.28 (t, 2H), 3.57 (s, 3H), 4.43 (s, 2H), 7.33 (d, 2H), 7.95 (d, 2H).

[0242] Step 2:

[0243] A stirred mixture of 53 (767 mg, 2.29 mmol), 1N LiOH (2.8 ml) and MeOH (15 ml) was kept at ambient temperature for 5 h, treated with additional LiOH (1 ml) and water (2.8 ml), kept at ambient temperature for 2h and concentrated in vacuo to remove MeOH. It was cooled in an ice bath, acidified with 1N HCl (4 ml) and extracted with CH₂Cl₂. The extract was washed with brine, dried (MgSO₄) and concentrated to give 613 mg of 15, a white foam: ¹H NMR [300 MHz, (CD₃)₂SO) δ 1.35, 1.41 (s, s, 9H), 2.56 (t, 2H), 2.76 (s, 3H), 3.22 (t, 2H), 4.43 (s, 2H), 7.33 (d, 2H), 7.95 (d, 2H), 12.12. (s, 1H).

[0244] Step 3:

[0245] An ice cold, stirred mixture of 15 (715 mg, 2.22 mmol), 16 (748 mg, 2.22 mmol), HOBT (330 mg, 2.44 mmol) and DMF (18 ml) was treated with EDC (936 mg, 4.88 mmol) and allowed to warm slowly to ambient temperature and stand for 18 h. It was concentrated in vacuo and the residue was chromatographed on silica gel with 4% MeOH-0.4% NH₄OH—CH₂Cl₂ to give 878 mg of 59, a white solid: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.35, 1.42 (s,s, 9H), 1.81 (s, 3H), 2.73 (m, 2H), 2.77 (s, 3H), 2.89, 2.99 (s, s, 4H), 3.22 (m, 2H), 3.38 (m, 2H), 3.57 (s, 2H), 3.66 (m, 3H), 4.07 (t, 1H), 4.43 (s, 2H), 4.69 (m, 1H), 7.07 (t, 1H), 7.15 (d, 1H), 7.33 (d, 2H), 7.48 (d, 1H), 7.96 (d, 2H), 8.24 (m, 1H): MS (EI) m/z 639.2 (M⁺), 335.1, 307.1, 306.1, 249.1, 248.1, 204.1; IR (drift) 3315, 1743, 1692, 1646 cm⁻¹.

[0246] Step 4:

[0247] Solid 59 (616 mg, 0.963 mmol) was cooled in an ice bath and treated with 4N HCl in dioxane (10 ml). The stirred mixture was kept in the ice bath for 1 h and at ambient temperature for 30 min. It was then concentrated in vacuo. The residue was mixed with water (10 ml) and saturated NaHCO₃ (10 ml) and extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Crystallization of the residue from CH₂Cl₂-MeOH-hexane gave 427 mg of 60: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.81 (s, 3H), 2.24 (s, 3H), 2.72 (m, 2H), 2.89, 2.99 (s, s, 4H), 3.22 (t, 2H), 3.32 (broad s), 3.38 (t, 2H), 3.57 (s, 2H), 3.68 (m, 5H), 4.07 (t, 1H), 4.69 (m, 1H), 7.07 (t, 1H), 7.17 (dd, 1H), 7.46 (m, 3H), 7.92 (d, 2H), 8.23 (t, 1H).

Example 20 N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-piperazin-1-yl]-4-oxobutanoyl}benzyl-N¹-methylglycinamide (65)

[0248] Step 1:

[0249] A solution of 41 (1.00 g of an 85:15 mixture of 41 and 42) in THF (10 ml) was added during 10 min to a stirred 2M solution of methylamine in THF (35 ml), kept at ambient temperature for 1 h and concentrated in vacuo. A solution of the residue in dilute HCl was washed with Et₂O and then made alkaline with solid NaHCO₃. It was extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated to give 538 mg of 41: ¹H NMR [300 MHz, (CD₃)₂SO] δ 2.23 (s, 3H), 2.63 (t, 2H), 3.27 (t, 2H), 3.57 (s, 3H), 3.69 (s, 2H), 7.44 (d, 2H), 7.91 (d, 2H); MS (EI) m/z 235.1 (M⁺), 205.1, 204.1, 1.62.1, 148.1, 120.0; IR (drift) 3331, 1738, 1685 cm⁻¹.

[0250] Step 2:

[0251] A stirred, ice cold solution of 61 (509 mg, 2.16 mmol), N-t-Boc-glycine (378 mg, 2.16 mmol) and HOBT (321 mg, 2.38 mmol) in DMF (18 ml) was treated with EDC (912 mg, 4.76 mmol), warmed slowly to ambient temperature and kept for 18 h. It was concentrated in vacuo and the residue was mixed with water and extracted with Et₂O. The extract was dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with 40-50% EtOAc-heptane gave 765 mg of 62, an oil: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.34, 1.37 (s, s, 9H), 2.63 (t, 2H), 2.81, 2.90 (s, s, 3H), 3.28 (t, 2H), 3.57 (s, 3H), 3.76, 3.84 (d, d, 2H), 4.56, 4.62 (s, s, 2H), 6.80 (m, 1H), 7.33 (d, 2H), 7.92, 7.98 (d, d, 2H); IR (drift) 3419, 3362, 1737, 1714, 1687, 1658 cm⁻¹.

[0252] Step 3:

[0253] A stirred mixture of 62 (701 mg, 1.79 mmol) and MeOH (12 ml) was treated with 1N LiOH (2.2 ml) and kept at ambient temperature for 5 h. Additional water (2.2 ml) and LiOH (1 ml) were added and the mixture was kept at ambient temperature for about 6 h and concentrated to remove MeOH. This mixture was cooled in an ice bath, acidified with 1N HCl and extracted with CH₂Cl₂. The extract was washed with brine, dried (MgSO₄) and concentrated to give 616 mg of 63, a white foam: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.34, 1.37 (s, s, 9H), 2.55 (t, 2H), 2.80, 2.90 (s, s, 3H), 3.21 (t, 2H), 3.77, 3.84 (d, d, 2H), 4.56, 4.62 (s, s, 2H), 6.81 (m, 1H), 7.33 (d, 2H), 7.92, 7.97 (d, d, 2H).

[0254] Step 4:

[0255] An ice cold, stirred mixture of 63 (555 mg, 1.47 mmol), 17b (493 mg, 1.47 mmol), HOBT (219 mg, 1.62 mmol) and DMF (12 ml) was treated with EDC (620 mg, 3.23 mmol), allowed to warm slowly to ambient temperature and kept for 18 h. It was concentrated in vacuo and the residue was chromatographed on silica gel with 5% MeOH-0.5% NH₄OH—CH₂Cl₂. The product was crystallized from CH₂Cl₂-MeOH-hexane to give 756 mg of 64: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.34, 1.37 (s, s, 9H), 1.81 (s, 3H), 2.73 (m, 2H), 2.81, 2.90 (s, s, 3H), 2.90, 2.99 (s, s, 4H), 3.21 (m, 2H), 3.38 (t, 2H), 3.57, 3.66 (s, s, 4H), 3.68 (m, 1H), 3.78, 3.84 (d, d, 2H), 4.07 (t, 1H), 4.57, 4.63 (s, s, 2H), 4.70 (m, 1H), 6.81 (m, 1H), 7.07 (t, 1H), 7.15 (dd, 1H), 7.33 (d, 2H), 7.49 (dd, 1H), 7.93, 7.98 (d, d, 2H), 8.23 (t, 1H); MS (FAB) m/z 697 (M+H⁺), 696 (M⁺), 597.3, 337.1, 261.1, 204.1; HRMS (FAB) calcd for C₃₅H₄₅FN₆O₈ (M⁺) 696.3282, found 696.3293.

[0256] Step 5:

[0257] Solid 64 (400 mg, 0.574 mmol) was cooled in an ice bath and treated with 4N HCl in dioxane (10 ml). The stirred mixture was kept in the ice bath for 1 h and at ambient temperature for 30 min and then concentrated in vacuo. A mixture of the residue in water (10 ml) and saturated NaHCO₃ (10 ml) was extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Crystallization of the residue from CH₂Cl₂-EtOAc-hexane gave 281 mg of 65: MS (EI) m/z 596 (M⁺), 552.3, 510.3, 495.3, 336.2, 306.2, 294.2, 250.3, 151.1; IR (drift) 3541, 3372, 3326, 1743, 1686, 1646 cm⁻¹. Anal. calcd for C₃₀H₃₇FN₆O₆: C, 60.39; H, 6.25; N, 14.09. Found: C, 60.08; H, 6.88; N, 13.75.

Example 21 N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)-N¹,N²,N²-trimethylglycinamide (68)

[0258] Step 1:

[0259] A stirred, ice cold mixture of 61 (509 mg, 2.16 mmol), HOBT (321 mg, 2.38 mmol), N,N-dimethylglycine (222 mg, 2.16 mmol) and DMF (18 ml) was treated with EDC (912 mg, 4.76 mmol) and allowed to warm slowly to ambient temperature. It was kept at this temperature for 18 h and concentrated in vacuo. The residue was chromatographed on silica gel with 4% MeOH-0.4% NH₄OH—CH₂Cl₂ to give 578 mg of 62, a yellow oil: ¹H NMR [300 MHz, (CD₃)₂SO] δ 2.15, 2.20 (s, s, 6H), 2.63 (t, 2H), 2.74, 2.97 (s, s, 3H), 3.08, 3.13 (s, s, 2H), 3.27 (t, 2H), 3.57 (s, 3H), 4.54, 4.74 (s, s, 2H), 7.34 (m, 2H), 7.95 (m, 2H); MS (EI) m/z 320.1 (M⁺), 289.1, 205.0, 146.0, 119.0, 118.0.

[0260] Step 2:

[0261] A stirred mixture of 66 (541 mg, 1.69 mmol), 1M lithium hydroxide (2.0 ml) and MeOH (11 ml) was kept at ambient temperature for 18 h, treated with additional LiOH (0.5 ml) and kept ambient temperature for 8 h. It was concentrated to dryness in vacuo and the residue was triturated with Et₂O to give 67 a white solid: ¹H NMR [300 MHz, (CD₃)₂SO] δ 2.15, 2.19 (s, s, 6H), 2.24 (t, 3H), 2.73, 2.95 (s, s, 3H), 3.07 (m, 4H), 3.39 (s, 3H), 4.52, 4.72 (s, s, 2H), 7.29 (m, 2H), 7.89 (m, 2H); MS (FAB) m/z 313 (M+H⁺); HRMS (FAB) calcd for C₁₆H₂₂LiN₂O₄ (M+H⁺) 313.1739, found 313.1739.

[0262] Step 3:

[0263] A stirred, ice cold mixture of 67 (468 mg, 1.50 mmol), 17b (505 mg, 1.50 mmol), HOBT (223 mg, 1.65 mmol) and DMF (12 ml) was treated with EDC (633 mg, 3.30 mmol) and allowed to warm slowly to ambient temperature. It was kept at this temperature for 24 h and concentrated in vacuo. The residue was mixed with water and extracted with EtOAc. The extract was dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄0H—CHCl₃ and crystallization of the product from EtOAc-CH₂Cl₂-hexane gave 638 mg of 68, a white solid: MS (EI) m/z 580.4, 565.3, 552.3, 335.2, 306.2; MS (CI) m/z 625 (M+H⁺); IR (drift) 3306, 1743, 1688, 1645 cm⁻¹. Anal. calcd for C₃₂H₄₁FN₆O₆: C, 61.52; H, 6.61;N, 13.45. Found: C, 61.10; H, 6.71;N, 13.32.

Example 22 N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)-N²,N²-dimethylglycinamide (75)

[0264] Step 1:

[0265] A stirred mixture of 41 (16.7 g of a 9:1 mixture of 41 and 42), sodium azide (22.3 g, 343 mmol) and DMF (84 ml) was warmed at 40-45° C. for 4 h and diluted with EtOAc (200 ml). It was washed with water, dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with 10-30% EtOAc-5% CH₂Cl₂-heptane gave 12.1 g of 69: mp 29-30° C.; ¹H NMR (300 MHz, CDCl₃) δ 2.77 (t, 2H), 3.32 (t, 2H), 3.71(s, 3H), 4.42 (s, 2H), 7.42 (d, 2H), 8.00 (d, 2H); MS (EI) m/z 247.0 (M⁺), 216.0, 205.0, 160.0, 132.0, 104.0; IR (drift) 2103, 1735, 1686 cm⁻¹.

[0266] Step 2:

[0267] A stirred mixture of 23 (12.0 g, 48.5 mmol) and MeOH (320 ml) was treated with 1N LiOH (53.4 ml) and kept at ambient temperature for 21 h. Additional LiOH (2.6 ml) was added and the mixture was kept at ambient temperature for 4 h and concentrated in vacuo to remove MeOH. The resulting aqueous solution was acidified with 1N HCl and extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Trituration of the residue with 10% EtOAc-heptane (100 ml) gave 10.04 g of 24: ¹H NMR (300 MHz, CDCl₃) δ 2.82 (t, 2H), 3.32 (t, 2H), 4.43 (s, 2H), 7.42 (d, 2H), 8.00 (d, 2H).

[0268] Step 3:

[0269] An ice cold, stirred mixture of 70 (10.0 g, 42.9 mmol), 17a (16.92 g, 42.9 mmol), HOBT (6.38 g, 47.2 mmol), and DMF (377 ml) was treated with EDC (18.1 g, 94.4 mmol) and kept for 4 h. It was diluted with water (1 L) and mixed with 1:1 Et₂O-heptane (500 ml). The solid was collected by filtration, washed with water and heptane and dried. Recrystalization from CH₂Cl₂-heptane gave 20.0 g of 71: mp 160-160.5° C.; ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.34 (s, 9H), 2.74 (t, 2H), 2.90, 3.00 (s, s, 4H), 3.24 (m, 4H), 3.58, 3.66 (s, s, 4H), 3.74 (dd, 1H), 4.07 (t, 1H), 4.56 (s, 2H), 4.66 (m, 1H), 7.07 (t, 1H), 7.17 (m, 2H), 7.49 (m, 3H), 8.00 (d, 2H); MS (EI) m/z 609.2 (M⁺), 308.1, 165.0, 153.1, 138.0, 137.0; IR (drift) 3376, 2132, 2095, 1788, 1732, 1685, 1652 cm⁻¹.

[0270] Step 4:

[0271] A mixture of 71 (4.97 g, 8.15 mmol), 10% palladium-on-carbon catalyst (1.25 g) and THF (300 ml) was hydrogenated at an initial pressure of 45 psi for 1.5 h. The flask was evacuated and refilled with hydrogen (45 psi) and the reaction was continued for 2 h. The mixture was filtered through celite; the solid was washed well with THF and the filtrate was concentrated in vacuo to give 4.95 g of 72, a white foam: IR (drift) 3320, 1753, 1710, 1684, 1645 cm⁻¹.

[0272] Step 5:

[0273] An ice cold, stirred mixture of 72 (2.00 g, 3.43 mmol), N,N-dimethylglycine (354 mg, 3.43 ml), HOBT (510 mg, 3.77 mmol) and DMF (30 ml) was treated with EDC (1.45 g, 7.55 mmol) and kept for 3 h. It was then diluted with water (50 ml) and extracted (emulsions) with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated to dryness in vacuo. Chromatography of the residue on silica gel with 5% MeOH—CH₂Cl₂ gave 473 mg of 73: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.33 (s, 9H), 2.21 (s, 6H), 2.72 (m, 2H), 2.89, 2.99 (s, s, 4H), 2.93 (s, 2H), 3.23 (m, 4H), 3.57, 3.66 (s, s, 4H), 3.74 (dd, 1H), 4.06 (t, 1H), 4.33 (d, 2H), 4.67 (m, 1H), 7.07 (t, 1H), 7.18 (m, 2H), 7.37 (d, 2H), 7.47 (dd, 1H), 7.92 (d, 2H), 8.41 (t, 1H).

[0274] Step 6:

[0275] Solid 73 (356 mg, 0.532 mmol) was cooled in an ice bath and treated with 4N HCl in dioxane (10 ml). The stirred mixture was kept in the ice bath for 2 h and at ambient 5 temperature for 1 h and then concentrated in vacuo. Four portions of CH₂Cl₂ (25 ml) were added to the residue with concentration after each addition to give 451 mg of 74, as an off-white solid: ¹H NMR [300 MHz, (CD₃)₂SO] δ 2.73 (m, 2H), 2.79, 2.81 (s, s, 6H), 2.90, 3.00 (s, s, 4H), 3.22 (m, 4H), 3.54, 3.66 (s, s, 4H), 3.86 (dd, 1H), 4.01 (d, 2H), 4.14 (t, 1H), 4.41 (d, 2H), 4.95 (m, 1H), 6.22 (broad s, 4H), 7.15 (m, 2H), 7.42 (d, 2H), 7.48 (dd, 1H), 7.94 (d, 2H), 8.49 (s, 3H), 9.36 (t, 1H), 10.02 (broad s, 1H).

[0276] Step 7:

[0277] A stirred, ice cold solution of 74 (about 0.357 mmol) in pyridine (8 ml) was treated with acetic anhydride (47 μL, 0.497 mmol) and allowed to warm to ambient temperature during 1 h. It was kept at ambient temperature for 1 h and concentrated in vacuo. Chromatography of the residue on silica gel first with 5% MeOH-0.5% NH₄OH—CH₂Cl₂ and then with 2.5% MeOH-0.5% NH₄OH—CH₂Cl₂ and crystallization of the product from MeOH gave 56 mg of 75: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.81 (s, 3H), 2.20 (s, 6H), 2.72 (t, 2H), 2.91 (m, 4H), 2.99 (s, 2H), 3.21 (t, 2H), 3.38 (t, 2H), 3.57 (s, 2H), 3.66 (m, 3H), 4.07 (t, 1H), 4.33 (d, 2H), 4.69 (m, 1H), 7.07 (t, 1H) 7.16 (dd, 1H), 7.37 (d, 2H), 7.48 (dd, 1H), 7.91 (d, 2H), 8.23 (t, 1H), 8.40 (t, 1H); MS (EI) m/z 610.2 (M⁺), 335.1, 306.1, 106.1; HRMS calcd for C₃₁H₄₀FN₆O₆ (M+H⁺) 611.2993, found 611.2996.

Example 23 N¹-(4-{4-[4-[2-Fluoro-4-{(5S)-2-oxo-5-[(propanethiolylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)-N²,N²-dimethylglycinamide (76)

[0278]

[0279] A stirred solution of 74 (270 mg, about 0.318 mmol) in MeOH (15 ml) was cooled in an ice bath and treated with Et₃N (0.46 ml, 3.31 mmol) and ethyl dithiopropionate (111 mg, 0.828 mmol). It was kept at ambient temperature for 18 h, adsorbed on silica gel (2 g) and chromatographed on silica gel with 5% MeOH-0.5% NH₄OH—CH₂Cl₂. The product was crystallized from MeOH-acetone-Et₂O to give 130 mg of 76, a white solid: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.12 (t, 3H), 2.57 (q, 2H), 2.73 (t, 2H), 2.80 (s, 6H), 2.89, 3.00 (s, s, 4H), 3.22 (t, 2H), 3.57, 3.66 (s, s, 4H), 3.80 (dd, 1H), 3.89 (m, 2H), 4.00 (s, 2H), 4.11 (t, 1H), 4.42 (d, 2H), 4.94 (m, 1H), 7.07 (t, 1H), 7.18 (dd, 1H), 7.42 (d, 2H), 7.48 (dd, 1H), 7.94 (d, 2H), 9.27 (t, 1H), 9.90 (s, 1H), 10.40 (t, 1H).

Example 24a (S)—N¹-(4-{4-[4-(2-Fluoro-4-{(5S)-2-oxo-5-[(propanethioylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)alaninamide (80)

[0280] Step 1:

[0281] An ice cold, stirred solution of 72 (1.44 g, 2.46 mmol) and Hunig's base (0.48 ml, 2.71 mmol) in CH₂Cl₂ (25 ml) and THF (25 ml) was treated with N-Fmoc-L-alanyl chloride (894 mg, 2.71 mmol) and kept in the ice bath for 1 h. The solid mixture was mixed with additional CH₂Cl₂ (15 ml) and kept at ambient temperature for 18 h. It was then treated with about 20 ml of heptane and filtered to give 1.672 g of 29: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.25 (d, 3H), 1.34 (s, 9H), 2.71 (t, 2H), 2.89, 2.99 (s, s, 4H), 3.23 (m, 4H), 3.57, 3.66 (s, s, 4H), 3.74 (dd, 1H), 4.06 (m, 2H), 4.24 (m, 3H), 4.34 (d, 2H), 4.66 (m, 1H), 7.07 (t, 1H), 7.18 (m, 2H), 7.35 (m, 6H), 7.48 (dd, 1H), 7.58 (d, 1H), 7.72 (m, 2H), 7.89 (m, 4H), 8.48 (t, 1H).

[0282] Step 2:

[0283] Solid 77 (940 mg, 1.07 mmol) was cooled in an ice bath and treated with 4N HCl in dioxane (10 ml). The mixture was stirred in the ice bath for 1 h and at ambient temperature for 1 h and concentrated in vacuo. The residue was mixed with four 25 ml portions of CH₂Cl₂ with concentration after each addition to give a white solid. A mixture of this material in saturated NaHCO₃ (20 ml) was extracted first with CH₂Cl₂ then with 5% MeOH—CH₂Cl₂ and finally with EtOAc. The extracts were dried and concentrated. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄OH—CHCl₃ gave 562 mg of 78, a white solid: MS (ESI) m/z 777.4 (M+H⁺), 577.1, 484.2; IR (drift) 3283, 1749, 1682, 1650, 1608 cm⁻¹.

[0284] Step 3:

[0285] A stirred mixture of 78 (641 mg, 0.825 mmol), triethylamine (0.29 ml, 2.07 mmol), ethyl dithiopropionate (155 mg, 1.16 mmol), MeOH (15 ml) and CH₂Cl₂ (5 ml) was kept at ambient temperature for 3 h. Additional triethylamine (0.2 ml) and dithioester (100 mg) were added and the reaction was continued for an additional 2 h. The mixture was then mixed with CH₂Cl₂ (50 ml) and silica gel (2 g) and concentrated. Chromatography of the residue on silica gel with 2.5% MeOH—CH₂Cl₂ and trituration of the product with a mixture of EtOAc-MeOH—CH₂Cl₂-Et₂O gave 400 mg of 79, a white solid: MS (ESI) m/z 849.0 (M+H⁺), 871.0 (M+Na⁺), 887.0 (M+K⁺); IR (drift) 3305, 1759, 1688, 1676, 1654, 1635 cm⁻.

[0286] Step 4:

[0287] A stirred mixture of 79 (380 mg, 0.448 mmol), trisamine resin (400 mg, 1.6 mmol) and THF (100 ml) was refluxed for 5 d. Additional resin (250 mg) was added and the mixture was refluxed for 8 h and filtered. The filtrate was treated with silica gel (2 g) and concentrated. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄OH—CHCl₃ and crystallization of the product from EtOAc-MeOH-heptane gave 228 mg of 80, a white solid: MS (FAB) m/z 627.3 (M+H⁺), 261.1; HRMS (FAB) calcd for C₃₁H₄₀FN₆O₅S (M+H⁺) 627.2765, found 627.2767; IR (drift) 3317, 3286, 1761, 1672, 1648, 1633cm⁻¹. Anal. calcd for C₃₁H₃₉FN₆O₅S: C, 59.41; H, 6.27; N, 13.41. Found: C, 58.58;H, 6.18;N, 13.15.

Example 24b (S)—N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-2-oxobutanoyl}benzyl)alaninamide (82)

[0288] Step 1:

[0289] A stirred mixture of 78 (500 mg, 0.644 mmol), triethylamine (0.72 ml, 5.15 mmol), CH₂Cl₂ (6.5 ml) and THF (6.5 ml) was treated with acetyl chloride (84 μL, 0.966 mmol) and kept at ambient temperature for 2 h. Additional acetyl chloride (45 μL) was added and the mixture was kept at ambient temperature for 18 h. It was then treated with silica gel (1.5 g) and concentrated. Chromatography of the residue on silica gel with 2.5% MeOH—CH₂Cl₂ gave the product (370 mg) which was further purified by preparative TLC on silica gel with 2.5% MeOH—CH₂Cl₂ to give 323 mg of 81, a white solid: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.25 (d, 3H), 1.82 (s, 3H), 2.72 (m, 2H), 2.90, 3.00 (s, s, 4H), 3.14 (m, 2H), 3.38 (t, 2H), 3.62 (m, 5H), 4.07 (m, 2H), 4.25 (m, 3H), 4.33 (d, 2H), 4.70 (m, 1H), 7.30 (m, 10H), 7.72 (m, 2H), 7.89 (m, 4H), 8.21 (t, 1H), 8.47 (t, 1H).

[0290] Step 2:

[0291] A stirred mixture of 81 (300 mg, 0.366 mmol), trisamine resin (91 mg) and THF (30 ml) was refluxed for 2 h and treated with additional resin (100 mg). It was refluxed for 18 h, treated with additional resin (200 mg) and refluxed for 8 h. Additional resin (200 mg) was again added and the mixture was refluxed for 18 h. The reaction was now complete; the mixture was filtered and the filtrate was concentrated. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄OH—CHCl₃ and crystallization of the product from Et₂O-EtOAc-heptane gave 151 mg of 82: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.14 (d, 3H), 1.81 (s, 3H), 2.26 (broad s, 2H), 2.72 (t, 2H), 2.90, 3.00 (s, s, 4H), 3.21 (t, 2H), 3.00 (m, 1H), 3.38 (t, 2H), 3.63 (m, 5H), 4.07 (t, 1H), 4.33 (d, 2H), 4.68 (m, 1H), 7.07 (t, 1H), 7.15 (dd, 1H), 7.37 (d, 2H), 7.49 (dd, 1H), 7.92 (d, 2H), 8.21 (t, 1H), 8.40 (t, 1H).

Example 25 N¹-(4-{4-[4-(2-Fluoro-4-{(5S)-2-oxo-5-[(propanethioylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)glycinamide (85)

[0292] Step 1:

[0293] An ice cold, stirred mixture of 72 (957 mg, 1.64 mmol), diisopropylethylamine (Hunig's base, HB, 0.316 ml, 1.77 mmol) and THF (33 ml) was treated, portionwise during about 1 min, with Fmoc glycyl chloride (559 mg, 1.77 mmol). The mixture was allowed to warm slowly to ambient temperature and stand for 18 h. It was then concentrated in vacuo, and the residue was chromatographed on silica gel with 3% MeOH—CH₂Cl₂. Impure fractions were triturated with EtOAc-heptane and rechromatographed with 2.5% MeOH—CH₂Cl₂. The product was crystallized from EtOAc-heptane to give 600 mg of 83: MS (ESI) m/z 862.9 (M+H⁺), 885.0 (M+Na⁺); IR (drift) 3353, 3329, 1741, 1728, 1710, 1691, 1682, 1652 cm⁻¹.

[0294] Step 2:

[0295] a) Ice cold, stirred 4N HCl in dioxane (10 ml) was treated, portionwise during 2 min with 83 (500 mg, 0.579 mmol). The mixture was kept in the ice bath for 1 h and at ambient temperature for 1 h and then concentrated in vacuo. The residue was triturated with three 50 ml portions of CH₂Cl₂ with concentration after each addition to give a white solid: MS (EI) m/z 762.5 (M⁺); IR (drift) 3289, 3240, 1762, 1726, 1716, 1676, 1663, 1657, 1645, 1632, 1628, 1608 cm⁻¹.

[0296] b) A mixture of the solid of step a) (463 mg), triethylamine (242 μL, 1.74 mmol), ethyl dithiopropionate (93 mg, 0.695 mmol) and MeOH (10 ml) was stirred at ambient temperature for 18 h. Additional MeOH (5 ml), triethylamine (242 μL) and dithioester (93 mg) were added to the mixture which was stirred for an additional 24 h. It was warmed at 50° C. for 1.5 h then diluted with CH₂Cl₂ (15 ml) and stirred at ambient temperature for 4 h. This mixture was diluted with CH₂Cl₂ (100 ml) adsorbed on silica gel and chromatographed on silica gel with 3.5% MeOH—CH₂Cl₂. The product was crystallized from EtOAc-CH₂Cl₂-heptane to give 218 mg of 84, as a white powder: MS (ESI) m/z 835.0 (M+H⁺), 857.0 (M+Na⁺); IR (drift) 3287, 1753, 1749, 1743, 1728, 1710, 1691, 1680, 1663, 1656, 1645, 1639, 1635 cm⁻.

[0297] Step 3:

[0298] A stirred solution of 84 (150 mg, 0.180 mmol) in DMF (1.8 ml) was treated with piperidine (45 μL), kept at ambient temperature for 30 min and concentrated in vacuo. The residue was chromatographed on silica gel with 5% MeOH—CH₂Cl₂. The resulting product was combined with the product from a similar 0.0599 mmol reaction and rechromatographed on silica gel with 5% MeOH-0.5% NH₄OH—CHCl₃. Crystallization of the product from Et₂O—CH₂Cl₂ gave 74.8 mg of 85: MS (EI) m/z 612.5 (M⁺), 568.3, 511.2, 321.6, 280.1, 259.1, 247.0, 208.4, 191.5, 164.4; HRMS (FAB) calcd for C₃₀H₃₈FN₆O₅S (M+H⁺) 613.2608, found 613.2607.

Example 26 (S)-Alanyl-(S)—N¹-(4-{4-[4-(2-fluoro-4-{(5S)-2-oxo-5-[(propanethioylamino)methyl]-1,3-oxazolidin-3-yl]phenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)alaninamide (89)

[0299] Step 1:

[0300] A stirred, ice cold mixture of 72 (2.00 g, 3.43 mmol), HOBT (510 mg, 3.77 mmol), N-Fmoc-L-alanyl-L-alanine (1.31 g, 3.43 mmol) and DMF (30 ml) was treated with EDC (1.45 g, 7.54 mmol) and allowed to warm slowly to ambient temperature. It was kept at ambient temperature for 4 h and diluted with about 500 ml of water. The resulting solid was collected by filtration, dried and chromatographed on silica gel with 5% MeOH—CH₂Cl₂ to give 2.22 g of 86: MS (ESI) m/z 948.0 (M+H⁺), 970.0 (M+Na⁺), 985.9 (M+K⁺); IR (drift) 3305, 1744, 1733, 1710, 1690, 1683, 1694, 1640 cm⁻¹.

[0301] Step 2:

[0302] Stirred, ice cold 4N HCl in dioxane (20 ml) was treated with 72 (2.21 g, 2.33 mmol) and the mixture was kept in the ice bath for 2 h and at ambient temperature for 1 h. It was then concentrated in vacuo and the residue was triturated with three 50 ml portions of CH₂Cl₂ with concentration after each addition. A mixture of the residue in saturated NaHCO₃ was extracted with CH₂Cl₂. A solid that formed during this process was collected by filtration, washed with water and dissolved in 20% MeOH—CH₂Cl₂. The organic solutions were dried (MgSO4) and concentrated to give 1.84 g of 63: MS (ESI) m/z 848.0 (M+H⁺), 869.9 (M+Na⁺), 886.4 (M+K⁺), 555.0, 467.0, 295.0; IR (drift) 3288, 1749, 1746, 1686, 1661, 1645, 1642 cm⁻¹.

[0303] Step 3:

[0304] A stirred mixture of 87 (600 mg, 0.708 mmol), triethylamine (236 μL, 1.69 mmol) and MeOH (8 ml) was treated with ethyl dithiopropionate (133 mg, 0.991 mmol) and kept at ambient temperature for 4 d. It was then diluted with CH₂Cl₂ to dissolve the solids, mixed with silica gel (5 g) and concentrated in vacuo. Chromatography of the residue on silica gel with 5% MeOH—CH₂Cl₂ gave 367 mg of 88, a white solid: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.13 (t, 3H), 1.22 (q, 6H), 2.57 (q, 2H), 2.72 (t, 2H), 2.90, 3.00 (s, s, 4H), 3.19 (t, 2H), 3.57, 3.66 (s, s, 4H), 3.79 (dd, 1H), 3.90 (t, 2H), 4.17 (m, 6H), 4.33 (d, 2H), 4.94 (m, 1H), 7.07 (t, 1H), 7.17 (dd, 1H), 7.42 (m, 8H), 7.69 (t, 2H), 7.88 (t, 4H), 8.02 (d, 1H), 8.41 (t, 1H), 10.28 (t, 1H).

[0305] Step 4:

[0306] A stirred mixture of 88 (330 mg, 0.359 mmol), trisamine resin (500 mg) and THF (30 ml) was refluxed for 24 h and filtered. The filtrate was concentrated and the residue was chromatographed on silica gel with 7% MeOH-0.7% NH₄OH—CHCl₃. Crystallization of the product from MeOH—CH₂Cl₂-heptane gave 151 mg of 89: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.14 (m, 6H), 1.25 (d, 3H), 2.27 (broad s, 2H), 2.58 (q, 2H), 2.74 (t, 2H), 2.92, 3.01 (s, s, 4H), 3.23 (t, 2H), 3.28 (m, 1H), 3.59, 3.68 (s, s, 4H), 3.81 (dd, 1H), 3.92 (t, 2H), 4.14 (t, 1H), 4.35 (m, 3H), 4.95 (m, 1H), 7.09 (t, 1H), 7.18 (dd, 1H), 7.38 (d, 2H), 7.52 (dd, 1H), 7.94 (d, 2H), 8.08 (m, 1H), 8.54 (t, 1H), 10.31 (t, 1H).

Example 27 (S)-Alanyl-(S)—N¹-(4-{4-[4-(4-{(5S)-5-[(acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)alaninamide (91)

[0307] Step 1:

[0308] A stirred mixture of 87 (304 mg, 0.359 mmol) and pyridine (6 ml) was treated with acetic anhydride (51 μL, 0.538 mmol) and kept at ambient temperature for 4 days. It was then concentrated to dryness in vacuo. The residue was combined with the product from a similar, 0.118 mmol reaction and 105 mg (0.114 mmol) was removed for a subsequent reaction. The remaining material was chromatographed on silica gel with 10% MeOH-1% NH⁴OH—CHCl₃ to give 218 mg of 90: MS (ESI) m/z 890.0 (M+H⁺), 912.0 (M+Na⁺), 928.0 (M+K⁺); IR (drift) 3289, 1744, 1687, 1645 cm^(—1).

[0309] Step 2:

[0310] A stirred mixture of 90 (200 mg, 0.225 mmol) and trisamine resin (550 mg) in THF (25 ml) was refluxed for 4 d, treated with additional resin (250 mg) and refluxed for 1 d. It was then filtered; the filtrate was concentrated and the residue was chromatographed on silica gel with 5% MeOH-0.5% NH₄OH—CHCl₃. The product was combined with the product from a similar 0.114 mmol reaction and crystallized from MeOH—CH₂Cl₂-heptane to give 164 mg of 91: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.12 (d, 3H), 1.23 (d, 3H), 1.81 (s, 3H), 2.72 (t, 2H), 2.89, 2.99 (s, s, 4H), 3.21 (t, 2H), 3.31 (m, 1H), 3.38 (t, 2H), 3.62 (m, 5H), 4.08 (t, 1H), 4.33 (m, 3H), 4.68 (m, 1H), 7.07 (t, 1H), 7.15 (d, 1H), 7.35 (d, 2H), 7.48 (d, 1H), 7.92 (d, 2H), 8.05 (s, 1H), 8.23 (t, 1H), 8.52 (t, 1H).

Example 28 N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}benzyl)acetamide (94)

[0311] Step 1:

[0312] A stirred solution of 72 (100 mg, 0.171 mmol) in pyridine (2.9 ml) was treated with acetic anhydride (24 μL, 0.257 mmol) and kept at ambient temperature for 1 h. It was then concentrated to dryness in vacuo. A solution of the residue in CH₂Cl₂ was treated with heptane to give 100 mg of 92, a white solid: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.34 (s, 9H), 1.87 (s, 3H), 2.72 (t, 2H), 2.89, 2.99 (s, s, 4H), 3.23 (m, 4H), 3.57, 3.66 (s, s, 4H), 3.74 (dd, 1H), 4.06 (t, 1H), 4.30 (d, 2H), 4.67 (m, 1H), 7.07 (t, 1H), 7.18 (m, 2H), 7.36 (d, 2H), 7.48 (dd, 1H), 7.92 (d, 2H), 8.43 (t, 1H).

[0313] Step 2:

[0314] Solid 92 (2.00 g, 3.20 mmol) was cooled in an ice bath, treated with 4N HCl in dioxane (20 ml) and stirred in the ice bath for 2 h and at ambient temperature for 1 h. It was then concentrated in vacuo. A solution of the residue in water (40 ml) was made alkaline with solid NaHCO₃ and extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. A solution of the residue in CH₂Cl₂-MeOH was treated with heptane and the solid that precipitated was collected by filtration and dried to give 1.45 g of 93: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.87 (s, 3H), 2.06 (broad s, 2H), 2.72 (t, 2H), 2.80 (t, 2H), 2.89, 2.99 (s, s, 4H), 3.21 (t, 2H), 3.57, 3.66 (s, s, 4H), 3.81 (dd, 1H), 4.01 (t, 1H), 4.30 (d, 2H), 4.59 (m, 1H), 7.07 (t, 1H), 7.20 (dd, 1H), 7.36 (d, 2H), 7.51 (dd, 1H), 7.92 (d, 2H), 8.43 (t, 1H).

[0315] Step 3:

[0316] A stirred solution of 93 (500 mg, 0.951 mmol) in pyridine (16 ml) was treated dropwise with acetic anhydride (135 μL, 1.43 mmol), kept at ambient temperature for 4 h and concentrated in vacuo. A mixture of the residue and water was extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Crystallization of the residue from MeOH gave 450 mg of 94, a white solid: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.81 (s, 3H), 1.87 (s, 3H), 2.72 (t, 2H), 2.89, 2.99 (s, s, 4H), 3.21 (t, 2H), 3.38 (t, 2H), 3.57 (s, 2H), 3.68 (m, 3H), 4.07 (t, 1H), 4.30 (t, 2H), 4.69 (m, 1H), 7.07 (t, 1H), 7.17 (dd, 1H), 7.36 (d, 2H), 7.49 (dd, 1H), 7.92 (d, 2H), 8.23 (t, 1H), 8.43 (t, 1H).

Example 29 N-(4-{4-[4-(2-Fluoro-4-{(5S)-2-oxo-5-[(propanethioylamino)methyl]-1,3-oxazolidin-3-yl]phenyl)-1-piperazinyl]-4-oxobutanoyl}benzyl)acetamide (95)

[0317]

[0318] A stirred solution of 93 (500 mg, 0.951 mmol), triethylamine (662 μL, 4.76 mmol), MeOH (20 ml) and CH₂Cl₂ (10 mL) was treated with ethyl dithiopropionate (384 mg, 2.86 mmol) and kept at ambient temperature for 3 days. It was concentrated in vacuo. A solution of the residue in CH₂Cl₂ was washed with 1N HCl and saturated NaHCO₃, dried (MgSO₄) and concentrated. The solid residue was triturated with EtOAc-heptane and then crystallized from MeOH to give 466 mg of 95: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.22 (t, 3H), 1.87 (s, 3H), 2.56 (q, 2H), 2.72 (t, 2H), 2.89, 2.99 (s, s, 4H), 3.21 (t, 2H), 3.57, 3.66 (s, s, 4H), 3.79 (dd, 1H), 3.90 (t, 2H), 4.11 (t, 1H), 4.30 (d, 2H), 4.93 (m, 1H), 7.07 (t, 1H), 7.17 (dd, 1H), 7.36 (d, 2H), 7.49 (dd, 1H), 7.92 (d, 2H), 8.43 (t, 1H), 10.29 (t, 1H).

Example 30 N-{[(5S)-3-(3-Fluoro-4-{4-[4-(4-{[(ethylsulfonyl)amino]methyl}phenyl)-4-oxobutanoyl]-1-piperazinyl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide (98)

[0319] Step 1:

[0320] Methanesulfonyl chloride (432 μL, 3.77 mmol) was added to a stirred solution of 72 (2.00 g, 3.43 mmol) in pyridine (4.0 ml) and the mixture was kept at ambient temperature for 4 h and concentrated in vacuo. The residue was mixed with water and extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. The residue was triturated with EtOAc to give 2.13 g of 96: MS (EI) m/z 661.3 (M⁺), 308.1; IR (drift) 3360, 3266, 1736, 1684, 1654 cm⁻¹.

[0321] Step 2:

[0322] Solid 96 (1.5 g, 2.27 mmol) was cooled, under nitrogen in an ice bath and treated with 4N HCl in dioxane (15 ml). The stirred mixture was kept in the ice bath for 1.5 h and at ambient temperature for 1.5 h and then concentrated in vacuo. A solution of the residue in water (25 ml) was made alkaline with NaHCO₃ and extracted with 1:5 MeOH:CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Crystallization of the residue from MeOH gave 1.00 g of 97: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.72 (broad s), 2.76 (m, 4H), 2.88 (s, 5H), 2.99 (s, 2H), 3.23 (t, 2H), 3.57, 3.66 (s, s, 4H), 3.81 (dd, 1H), 4.01 (t, 1H), 4.23 (s, 2H), 4.57 (m, 1H), 7.07 (t, 1H), 7.19 (dd, 1H), 7.49 (m, 3H), 7.67 (broad s, 1H), 7.96 (d, 2H).

[0323] Step 3:

[0324] A stirred solution of 97 (500 mg, 0.890 mmol) in pyridine (15 ml) was treated, dropwise with acetic anhydride (126 μL, 1.34 mmol) and kept at ambient temperature for 4 h. It was then concentrated in vacuo and the residue was mixed with water and extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Crystallization of the residue from MeOH gave 481 mg of 98: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.83 (s, 3H), 2.75 (t, 2H), 2.90 (s, 5H), 3.02 (s, 2H), 3.25 (t, 2H), 3.40 (t, 2H), 3.60 (s, 2H), 3.68 (m, 3H), 4.09 (t, 1H), 4.25 (d, 2H), 4.71 (m, 1H), 7.09 (t, 1H), 7.18 (dd, 1H), 7.51 (m, 3H), 7.69 (t, 1H), 7.98 (d, 2H), 8.25 (t, 1H).

Example 31 N-{[(5S)-3-(3-Fluoro-4-{4-[4-(4-{[(methylsulfonyl)amino]methyl}phenyl)-4-oxobutanoyl]-1-piperazinyl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}propanethioamide (99)

[0325]

[0326] A stirred mixture of 97 (500 mg, 0.890 mmol), triethylamine (310 ,L, 2.23 mmol), ethyl dithiopropionate (179 mg, 1.34 mmol), MeOH (20 ml) and CH₂Cl₂ (15 ml) was kept at ambient temperature for 2 h, treated with additional triethylamine (310 μL) and dithioester (179 mg) and kept at ambient temperature for 3 d. It was then treated with silica gel (5 g) and concentrated. Chromatography of the residue on silica gel with 4% MeOH—CH₂Cl₂ and crystallization of the product from MeOH gave 420 mg of 99, a white solid: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.15 (t, 3H), 2.59 (q, 2H), 2.75 (t, 2H), 2.90 (s, 3H), 2.91 (s, 2H), 3.02 (s, 2H), 3.25 (t, 2H), 3.60, 3.68, (s, s, 4H), 3.81 (dd, 1H), 3.92 (t, 2H), 4.14 (t, 1H), 4.24 (d, 2H), 4.96 (m, 1H), 7.09 (t, 1H), 7.20 (dd, 1H), 7.51 (m, 3H), 7.69 (t, 1H), 7.98 (d, 2H), 10.32 (t, 1H).

Example 32a N-({(5S)-3-[4-(4-{4-[4-(Aminomethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl)-3-fluorophenyl]-2-oxo-1,3-oxazolidin-S-yl}methyl)propanethioamide (103)

[0327] Step 1:

[0328] A stirred, ice cold mixture of 72 (2.46 mmol) and Hunig's base (0.48 ml, 2.71 mmol) in THF (49 ml) was treated with Fmoc-chloride (701 mg, 2.71 mmol) and allowed to warm slowly to ambient temperature and stand for 18 h. It was concentrated, without heating in vacuo and the residue was stirred with Et₂O (200 ml) and filtered. The solid was dried to give 2.10 g of 100 as an off-white solid: MS (ESI) m/z 806.1 (M+H⁺), 827.9 (M+Na⁺), 844.1 (M+K⁺); IR (drift) 3353, 1731, 1694, 1685, 1651 cm⁻¹.

[0329] Step 2:

[0330] Ice cold 4N HCl in dioxane (10 ml) was treated with 100 (1.00 g, 1.24 mmol) and the mixture was kept in the ice bath for 1 h and at ambient temperature for 3 h. It was then concentrated in vacuo. The residue was mixed with two portions of CH₂Cl₂ (50 ml) with concentration after each addition and the resulting material was mixed with saturated NaHCO₃ (20 ml) and extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated to give 689 mg of 101: MS (FAB) m/z 662.3 (M-CO₂+H⁺), 484.3, 356.1, 355.1, 295.2, 195.1, 179.1; HRMS (FAB) calcd for C₃₉H₄₁FN₅O₄ (M-CO₂+H⁺) 662.3142, found 662.3166; IR (drift) 3288, 1749, 1682, 1645 cm⁻¹.

[0331] Step 3:

[0332] A stirred mixture of 101 (668 mg, 0.946 mmol), triethylamine (330 μL, 2.37 mmol) and MeOH (10 ml) was treated with ethyl dithiopropionate (152 mg, 1.14 mmol) and CH₂Cl₂ (4 ml) and the resulting solution was kept at ambient temperature for 18 h. It was then mixed with silica gel (2 g) and concentrated in vacuo. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄OH—CH₂Cl₂ and crystallization of the product from EtOAc-heptane gave 445 mg of 102, a white solid: MS (CI) m/z 777.9 (M⁺), 619.9; IR (drift) 3306, 1756, 1744, 1692, 1645 cm⁻¹.

[0333] Step 4:

[0334] A stirred solution of 102 (340 mg, 0.437 mmol) in DMF (4.4 ml) was treated with piperidine (108 μL, 1.09 mmol), kept at ambient temperature for 30 min and concentrated in vacuo. The residue was chromatographed on silica gel with 5% MeOH-0.5% NH₄OH—CHCl₃ and the product was crystallized from EtOAc to give 192 mg of 103, a white solid: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.12 (t, 3H), 2.13 (broad s, 2H), 2.56 (q, 2H), 2.72 (t, 2H), 2.90, 3.00 (s, s, 4H), 3.22 (t, 2H), 3.58, 3.66 (s, s, 4H), 3.77 (m, 3H), 3.90 (s, 2H), 4.11 (t, 1H), 4.93 (m, 1H), 7.07 (t, 1H), 7.17 (dd, 1H), 7.47 (m, 3H), 7.91 (d, 2H), 10.29 (s, 1H).

Example 32b N-({(5S)-3-[4-(4-{4-[4-(Aminomethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl)-3-fluorophenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)propanethioamide (103)

[0335] Step 1:

[0336] A stirred, ice cold mixture of 72 (70 mg, 0.12 mmol), NaHCO₃ (12 mg, 0.14 mmol) and 3:1 acetone:H₂O (1 ml) was treated with benzyl chloroformate (20 μL, 0.14 mmol) and allowed to warm slowly to ambient temperature and stand for 18 h. It was then mixed with water (15 ml) and extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with 2% MeOH—CH₂Cl₂ and crystallization of the product from EtOAc-heptane gave 51 mg of 104: mp 158-159° C.; ¹H NMR (300 MHz, CDCl₃) δ 1.41 (s, 9H), 2.82 (t, 2H), 3.01, 3.09 (t, t, 4H), 3.36 (t, 2H), 3.51 (m, 2H), 3.79 (m, 5H), 4.00 (t, 1H), 4.44 (d, 2H), 4.73 (m, 1H), 4.95 (m, 1H), 5.12 (m, 1H), 5.15 (s, 2H), 6.92 (t, 1H), 7.08 (dd, 1H), 7.36 (m, 7H), 7.46 (dd, 1H), 7.98 (d, 2H).

[0337] Step 2:

[0338] Solid 103 (830 mg, 1.15 mmol) was cooled in an ice bath and treated with 4N HCl in dioxane (10 ml). The stirred mixture was kept in the ice bath for 1 h and at ambient temperature for 1 h and then concentrated in vacuo. The residue was triturated with three portions of CH₂Cl₂ (50 ml) with concentration after each addition. The resulting material was mixed with saturated NaHCO₃ (50 ml) and extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated to give 657 mg of 105, an off-white solid: ¹H NMR (300 MHz, CDCl₃) δ 2.82 (t, 2H), 3.04 (m, 6H), 3.35 (t, 2H), 3.65 (dd, 1H), 3.77 (m, 5H), 4.00 (t, 1H), 4.44 (d, 2H), 4.66 (m, 1H), 5.14 (s, 2H), 5.20 (m, 1H), 6.92 (t, 1H), 7.13 (dd, 1H), 7.36 (m, 7H), 7.49 (dd, 1H), 7.98 (d, 2H).

[0339] Step 3:

[0340] A stirred mixture of 105 (312 mg, 0.504 mmol), triethylamine (175 μL, 1.26 mmol), ethyl dithiopropionate (74 mg, 0.55 mmol) and MeOH (8 ml) was kept at ambient temperature for 18 h. Methylene chloride (5 ml) and additional dithioester (50 mg) were added and the mixture was kept at ambient temperature for 2 h and concentrated. The residue was stirred for 18 h with a mixture of water (50 ml) and 10% EtOAc-heptane. Chromatography of the resulting solid on silica gel first with 3% MeOH—CH₂Cl₂ and again with 2% MeOH—CH₂Cl₂ and crystallization of the product from EtOAc gave 241 mg of 106: MS (ESI) m/z 690.0 (M+H⁺), 711.9 (M+Na⁺), 727.9 (M+K⁺); IR (drift) 3343, 3202, 1743, 1694, 1646 cm⁻¹.

[0341] Step 4:

[0342] A stirred mixture of 106 (100 mg, 0.145 mmol) and 30% HBr in HOAc (5 ml) was kept at ambient temperature for 1 h and diluted with Et₂O (60 ml). The resulting solid was collected by filtration and washed with Et₂O. It was then mixed with water (15 ml) and saturated NaHCO₃ (15 ml) and extracted with CH₂Cl₂. The extract was dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with 2.5% MeOH-0.25% NH₄OH—CH₂Cl₂ and crystallization of the product from EtOAc gave 44 mg of 103, a white solid.

Example 33 N-({(5S)-3-[4-(4-{4-[4-(Aminomethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl)-3-fluorophenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide (108).

[0343] Step 1:

[0344] A stirred solution of 101 (755 mg, 1.07 mmol) and triethylamine (1.2 ml, 8.56 mmol) in THF (11 ml) and CH₂Cl₂ (11 ml) was treated with acetyl chloride (139 μL, 1.61 mmol) and kept at ambient temperature for 30 min. It was then mixed with water (30 ml) and extracted with CH₂Cl₂. The extract was washed with saturated NaHCO₃, dried (MgSO₄) and concentrated. Trituration of the solid residue with heptane that contained small amounts of acetone, Et₂O, MeOH and EtOAc gave 607 g of 107, a white solid: MS (ESI) m/z 748.0 (M+H⁺), 411.9, 231.9; IR (drift) 3305, 1744, 1687, 1646 cm⁻¹.

[0345] Step 2:

[0346] A stirred solution of 107 (576 mg, 0.770 mmol) in DMF (7.8 ml) was treated with piperidine (190 μL, 1.93 mmol), kept at ambient temperature for 30 min and concentrated in vacuo. Chromatography of the residue on silica gel with 5% MeOH-0.5% NH₄OH—CHCl₃ and crystallization of the product from MeOH—CH₂Cl₂-heptane gave a solid that turned yellow when dried at 50° C. It was dissolved in 1:1 CH₂Cl₂:MeOH (50 ml), decolorized with activated carbon and crystallized from CH₂Cl₂-MeOH-Et₂O to give 131 mg of 108: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.81 (s, 3H), 2.72 (t, 2H), 2.90, 3.00 (s, s, 4H), 3.22 (t, 2H), 3.30 (broad s), 3.38 (t, 2H), 3.58 (s, 2H), 3.66 (m, 3H), 3.81 (s, 2H), 4.07 (t, 1H), 4.68 (m, 1H), 7.07 (t, 1H), 7.16 (dd, 1H), 7.49 (m, 3H), 7.92 (d, 2H), 8.23 (t, 1H).

Example 34 N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)glycinamide (112).

[0347] Step 1:

[0348] A stirred, ice cold solution of 70 (1.79 g, 7.67 mmol), 17b (2.58 g, 7.67 mmol), HOBT (1.14 g, 8.44 mmol) and DMF (67 ml) was treated with EDC (3.23 g, 16.9 mmol) and kept in the ice bath for 2 h and at ambient temperature for 2 h. It was then mixed with water (500 ml) and 1:4 Et₂O:heptane (250 ml). The solid was collected by filtration, dried and chromatographed on silica gel with 5% MeOH—CH₂Cl₂ to give 3.51 g of 109: MS (EI) m/z 551.2 (M⁺), 335.1, 334.1, 307.1; IR (drift) 3307, 2100, 1743, 1688, 1647 cm⁻¹.

[0349] Step 2:

[0350] A mixture of 109 (1.50 g, 2.72 mmol), 10% palladium-on-carbon catalyst (375 mg) and THF (90 ml) was hydrogenated for 1 h at an initial pressure of 35 psi. The flask was evacuated and refilled with hydrogen and the reaction was continued for 1 h. Additional catalyst (200 mg) and CH₂Cl₂ (20 ml) were added to the mixture which was again hydrogenated for 1 h. This mixture was filtered and the filtrate was concentrated. Chromatography of the residue on silica gel with mixtures of MeOH—NH₄OH—CH₂Cl₂ that contained 5-10% MeOH and 0.5-1% NH₄OH gave 876 mg of 110, a white solid: MS (FAB) m/z 526.3 (M+H⁺), 337.2, 190.1; IR (drift) 3323, 1743, 1685, 1647 cm⁻¹. Anal. calcd for C₂₇H₃₂FN₅O₅.0.5 H₂O: C, 60.66; H, 6.22; N, 13.10. Found: C, 60.80; H, 6.22; N, 13.04.

[0351] Step 3:

[0352] Compound 110 (852 mg, 1.62 mmol) was dissolved in warm DMF (14 ml). The stirred solution was cooled in an ice bath and treated with N-t-Boc-glycine (284 mg, 1.62 mmol), HOBT (240 mg, 1.78 mmol) and finally EDC (682 mg, 3.56 mmol). It was kept in the ice bath for 2 h and at ambient temperature for 2 h and then mixed with water (150 ml). The resulting solid was collected by filtration, washed with water and then with 1:1 Et₂O-heptane and dried to give 998 mg of 111: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.37 (s, 9H), 1.81 (s, 3H), 2.72 (t, 2H), 2.89, 2.99 (s, s, 4H), 3.21 (t, 2H), 3.38 (t, 2H), 3.56 (m, 4H), 3.66 (m, 3H), 4.07 (t, 1H), 4.33 (d, 2H), 4.69 (m, 1H), 7.07 (m, 2H), 7.16 (dd, 1H), 7.37 (d, 2H), 7.49 (dd, 1H), 7.90 (d, 2H), 8.23 (t, 1H), 8.38 (t, 1H).

[0353] Step 4:

[0354] Solid 111 (830 mg, 1.22 mmol) was cooled in an ice bath under nitrogen, and treated with 4N HCl in dioxane (10 ml). The mixture was stirred in the ice bath for 1.5 h and then concentrated in vacuo. A solution of the residue in water (15 ml) was made alkaline with solid NaHCO₃ and freeze dried. The resulting solid was extracted with MeOH—CH₂Cl₂ and the extract was concentrated. Chromatography of the residue on silica gel with 10-20% MeOH—CH₂Cl₂ and crystallization of the product from MeOH—CH₂Cl₂-heptane gave 338 mg of 112, as an off-white solid: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.81 (s, 3H), 2.72 (t, 2H), 2.72 (broad s, 2H), 2.89, 2.99 (s, s, 4H), 3.18 (s, 2H), 3.21 (t, 2H), 3.38 (t, 2H), 3.57 (s, 2H), 3.68 (m, 3H), 4.07 (t, 1H), 4.35 (d, 2H), 4.69 (m, 1H), 7.07 (t, 1H), 7.17 (dd, 1H), 7.38 (d, 2H), 7.49 (dd, 1H), 7.92 (d, 2H), 8.24 (t, 1H), 8.46 (t, 1H).

Example 35 2-[3-methyl-3-(4-{(5S)-2-oxo-5-[(propionylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)azetidin-1-yl]-2-oxoethyl 4-(aminomethyl)benzamide (120).

[0355] Step 1:

[0356] A suspension of anhydrous K₂CO₃ (13.0 g, 94.3 mmol) in CH₃CN (175 mL) is treated with ethyl cyanoacetate (5.0 mL, 47.1 mmol) at rt with stirring. The reaction is warmed to 75° C. for 20 min, then cooled to 0° C. with an ice bath followed by dropwise treatment with 1-fluoro-4-nitrobenzene (5.0 mL, 47.1 mmol) over 5 min. The ice bath is removed and the red suspension is warmed to 75° C. for 18 h. The dark red suspension is then cooled to rt, treated with iodomethane (26.4 mL, 424.2 mmol), K₂CO₃ (19.5 g, 141.4 mmol), acetone (60 mL), and then warmed to 60° C. for 24 h. The pink suspension is then cooled to rt and filtered through Celite (repeated EtOAc washings). After concentrating the filtrate in vacuo, the orange-brown residue is diluted with H₂O (300 mL) and extracted with EtOAc (2×200 mL). The combined organic extracts are washed with brine (150 mL), dried over MgSO₄, and concentrated in vacuo. Purification of the crude product via Biotage chromatography (eluting with 20% EtOAc/Hexane) affords 113 (4.87 g) as a white solid. ¹H NMR (400 MHz, CDCl₃) δ 8.27 (d, J=8.9 Hz, 2 H), 7.73 (d, J=9.1 Hz, 2 H), 4.26 (m, 2 H), 1.99 (s, 3 H), 1.26 (t, J=7.2 Hz, 3 H).

[0357] Step 2:

[0358] A solution 113 (15.8 g, 63.8 mmol) in absolute EtOH (650 mL) is treated with Raney nickel (34.5 g of a 50% slurry in H₂O) and subjected to hydrogenation in a Parr apparatus for 18 h (25-30 psi H₂, rt). The reaction mixture is then filtered through Celite (repeated EtOH washings) and concentrated in vacuo. Purification of the crude product via Biotage chromatography (eluting with 15% MeOH/EtOAc) affords the reduced amino-aniline compound corresponding to 113 (11.36 g) as a pale yellow oil: ¹H NMR (400 MHz, CDCl₃) δ 7.04 (d, J=8.7 Hz, 2 H), 6.63 (d, J=8.7 Hz, 2 H), 4.13 (m, 2 H), 3.09 (d, J=13.3 Hz, 1 H), 2.94 (d, J=13.5 Hz, 1 H), 1.52 (s, 3 H), 1.19 (t, J=7.2 Hz, 3 H); ¹³C NMR (100 MHz, CDCl₃) δ 175.87, 145.17, 131.43, 127.06, 115.02, 60.61, 51.74, 51.14, 20.81, 14.05. A solution of this amino-aniline (8.3 g, 37.3 mmol) in THF (207 mL) is added dropwise to a 0° C. solution of methyl magnesium bromide (62.2 mL, 3.0 M in Et₂O) in THF (415 mL). When addition is complete, THF (30 mL) is used to rinse the addition funnel, and then the ice bath is removed and reaction stirred at rt for 3 h. The reaction contents are poured into saturated aqueous NH₄Cl (1000 mL) and volatiles are removed in vacuo. The aqueous phase is extracted with CHCl₃ (4×300 mL). The combined organic extracts are washed with H₂O (200 mL), brine (200 mL), dried over MgSO₄, and concentrated in vacuo. Purification of the crude product via Biotage chromatography (eluting with 50% EtOAc/hexane) affords 114 (4.65 g) as an off-white solid in 71% yield; ¹H NMR (300 MHz, CDCl₃) δ 7.17 (d, J=8.7 Hz, 2 H), 6.65 (d, J=8.3 Hz, 2 H), 6.13 (s, 1 H), 3.48 (d, J=5.3 Hz, 1 H), 3.36 (d, J=5.3 Hz, 1 H), 1.62 (s, 3 H); ¹³C NMR (100 MHz, CDCl₃) δ 173.44, 145.30, 130.60, 126.71, 115.15, 59.41, 51.40, 23.14; MS (ESI+) for C₁₀H₁₂N₂O m/z 177.1 (M+H)^(+.)

[0359] Step 3:

[0360] A solution of LiAlH₄ (79.2 mL, 1.0 M in THF) is diluted with THF (77 mL) and cooled to 0° C. To this is added a solution of 114 (4.65 g, 26.4 mmol) in THF (116 mL), with gas evolution. The ice bath is removed and the reaction was heated to reflux (75° C. oil bath) for 22 h, during which time the reaction became a white suspension. After cooling to rt, the mixture was treated successively with H₂O (3.01 mL), 5 N aqueous NaOH (2.71 mL), and H₂O (10.52 mL). The resulting suspension was diluted with EtOAc (600 mL), filtered through a pad of Celite, rinsing the Celite with additional EtOAc (400 mL). Concentration in vacuo affords the desired azetidine (4.76 g) as a yellow oil. A solution of this crude intermediate in acetone (85 mL) and H₂O (47 mL) was treated with sodium bicarbonate (19.96 g, 237.6 mmol). The resulting suspension was cooled to 0° C. and treated with benzylchloroformate (18.84 mL, 132.0 mmol) with gas evolution. The ice bath was removed and the reaction mixture was stirred overnight at rt. In the a.m., the reaction mixture was diluted with saturated aqueous sodium bicarbonate (200 mL) and extracted with EtOAc (3×200 mL). The combined organic extracts were washed with H₂O (100 mL), brine (100 mL), dried over MgSO₄, and concentrated in vacuo. Purification of the crude product via Biotage chromatography (eluting with 25% EtOAc/hexane) affords (4.75 g) as a pale yellow syrup; ¹H NMR (400 MHz, CDCl₃) δ 7.41-7.29 (m, 12 H), 7.13 (d, J=8.7 Hz, 2 H), 6.77 (s, 1 H), 5.19 (s, 2 H), 5.10 (s, 2 H), 4.22 (d, J=8.3 Hz, 2 H), 3.97 (d, J=8.3 Hz, 2 H), 1.59 (s, 3 H); MS (ESI−) for C₂₆H₂₆N₂O₄ m/z 429.0 (M−H)^(−.)

[0361] Step 4:

[0362] A solution of 116 (4.75 g, 11.03 mmol) in DMF (20 mL) at 0° C. is treated with LiOt-Bu (33.1 mL, 1.0 M solution in hexanes) dropwise over 25 min. After an additional 20 min, the reaction is treated with 116 (4.63 g, 22.07 mmol, U.S. patent Publication application Ser. No. 2002/0086900) and stirred 14 h with ice bath expiring. The reaction is quenched with saturated aqueous NH₄Cl (85 mL) and then extracted with EtOAc (3×80 mL). The combined organic extracts are washed with brine, dried over MgSO₄, and concentrated in vacuo. Purification of the crude product via Biotage chromatography (eluting with 50% EtOAc/hexane) affords 117 (4.16 g) as a white solid; ¹H NMR (400 MHz, DMSO-d₆) δ 7.50 (d, J=8.7 Hz, 2 H), 7.39-7.30 (m, 5 H), 7.31 (d, J=8.7 Hz, 2 H), 7.22 (t, J=5.9Hz, 1 H), 5.05 (s, 2 H), 4.68 (m, 1 H), 4.14 (m, 2 H), 4.10 (t, J=9.0 Hz, 1 H), 3.95 (m, 2 H), 3.78 (dd, J=9.0, 5.9 Hz, 1 H), 3.27 (t, J=5.4 Hz, 2 H), 1.54 (s, 3 H), 1.35 (s, 9 H); ¹³C NMR (100 MHz, DMSO-d₆) δ 155.86, 154.03, 141.54, 136.73, 136.56, 128.28, 127.75, 127.52, 125.73, 117.96, 77.96, 71.28, 65.62, 47.03, 42.79, 37.69, 28.79, 28.00.

[0363] Step 5:

[0364] A solution of 117 (4.10 g, 8.37 mmol) in MeOH (20 mL) at 0° C. is treated with 4 M HCl-dioxane (5.0 mL) and stirred for 10 min. The ice bath is then removed, and after stirring 20 h at rt, the solution is concentrated in vacuo. The resulting pale yellow solid is subsequently treated with pyridine (12 mL) and propionic anhydride (6 mL) in CH₂Cl₂ (30 mL) at 0° C. and stirred 14 h with bath expiring. The reaction is quenched with H₂O (150 mL), and the layers are separated. The organic layer is washed with 1.0 M HCl (2×50 mL), brine (50 mL), dried over MgSO₄, and concentrated in vacuo. Trituration (Et₂O) affords (2.98 g) as a white solid in 79% yield; ¹H NMR (400 MHz, DMSO-d₆) δ 8.18 (t, J=5.8 Hz, 1 H), 7.50 (d, J=8.7 Hz, 2 H), 7.39-7.30 (m, 5 H), 7.31 (d, J=8.5 Hz, 2 H), 5.05 (s, 2 H), 4.72 (m, 1 H), 4.13 (m, 2 H), 4.11 (t, J=8.9 Hz, 1 H), 3.96 (m, 2 H), 3.74 (dd, J=8.9, 6.2 Hz, 1 H), 3.42 (m, 2 H), 2.10 (q, J=7.7 Hz, 2 H), 1.54 (s, 3 H), 0.96 (t, J=7.7 Hz, 3 H); ¹³C NMR (100 MHz, DMSO-d₆) δ 173.65, 155.88, 154.04, 141.56, 136.74, 136.52, 128.29, 127.75, 127.53, 125.75, 117.98, 71.43, 65.64, 47.11, 41.24, 37.69, 28.78, 28.25, 9.81.

[0365] Step 6:

[0366] A solution of 118 (2.78 g, 6.16 mmol) in 5:1 MeOH:THF (60 mL) was placed under N₂ (g) and then treated with 10% Pd/C (278 mg). The reaction vessel was then charged with H₂ (g) and the reaction mixture was stirred overnight at rt. In the a.m., the mixture was filtered and concentrated in vacuo. Purification of the crude product via Biotage chromatography (eluting first with 10% MeOH/CH₂Cl₂ and then with 5-15% MeOH(NH₃)/CH₂Cl₂) affords (1.79 g) as a white solid; ¹H NMR (400 MHz, DMSO-d₆) δ 8.18 (t, J=5.8 Hz, 1 H), 7.47 (d, J=8.9 Hz, 2 H), 7.21 (d, J=8.7 Hz, 2 H), 4.71 (m, 1 H), 4.10 (t, J=9.0 Hz, 1 H), 3.74 (t, J=6.4 Hz, 1 H), 3.73 (d, J=6.6 Hz, 2 H), 3.42 (m, 2 H), 3.38 (d, J=7.5 Hz, 2 H), 2.10 (q, J=7.5 Hz, 2 H), 1.53 (s, 3 H), 0.96 (t, J=7.6 Hz, 3 H); ¹³C NMR (100 MHz, DMSO-d₆) δ 173.65, 154.06, 144.21, 135.92, 125.29, 117.95, 71.39, 58.27, 47.15, 41.91, 41.25, 28.64, 28.25, 9.82 1.41.

[0367] Step 7:

[0368] A solution of 119 (241 mg, 0.76 mmol) and N-(4-{[(tert-butoxycarbonyl)-amino[methyl}benzoyl)glycine (246 mg, 0.80 mmol) in CH₃CN (20 mL) at 0° C. was treated with HATU (304 mg, 0.80 mmol) followed by Hunig's base (0.70 mL, 3.99 mmol) and stirred overnight with ice bath expiring. In the a.m., the reaction mixture was concentrated in vacuo, and the residue dissolved in CH₂Cl₂ (200 mL). This organic phase was washed with H₂O, brine, dried over MgSO₄, and concentrated in vacuo to afford a yellow-brown solid. Purification via Biotage chromatography (eluting with 2-10% MeOH/CH₂Cl₂) affords the Boc-protected amine (352 mg) as a glassy film in 76% yield. This compound (300 mg) was subsequently treated with TFA (2.0 mL) in CH₂Cl₂ (7.0 mL) at 0° C. for 10 min, and then stirred an additional 2h at rt. Concentration in vacuo followed by purification via Biotage chromatography (eluting first with 10% MeOH/CH₂Cl₂ and then with 10% MeOH(NH₃)/CH₂Cl₂) affords 120 (217 mg) as a pale yellow; ¹H NMR (400 MHz, DMSO-d₆) δ 8.67 (t, J=5.7 Hz, 1 H), 8.19 (t, J=5.9 Hz, 1 H), 7.83 (d, J=8.3 Hz, 2 H), 7.53 (d, J=8.9 Hz, 2 H), 7.44 (d, J=8.3 Hz, 2 H), 7.34 (d, J=8.7 Hz, 2 H), 4.73 (m, 1 H), 4.45 (d, J=8.3 Hz, 1 H), 4.25 (d, J=8.3 Hz, 1 H), 4.12 (t, J=9.1 Hz, 1 H), 4.09 (d, J=9.1 Hz, 1 H), 3.90 (m, 3 H), 3.82 (s, 2 H), 3.76 (dd, J=9.0, 6.3 Hz, 1 H), 3.42 (m, 4 H), 2.10 (q, J=7.7 Hz, 2 H), 1.57 (s, 3 H), 0.96 (t, J=7.6 Hz, 3 H).

Example 36 N-{[(5S)-3-(4-{1-[4-(4-aminophenyl)-4-oxobutanoyl]-3-methylazetidin-3-yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}propanamide (121).

[0369]

[0370] A mixture of 119 (1.50 g, 4.73 mmol), 4-(4-aminophenyl)-4-oxobutanoic acid (1.10 g, 5.67 mmol), HOBt (703 mg, 5.20 mmol), and Hunig's base (2.06 mL, 11.83 mmol) in CH₂Cl₂ (25 mL) at 0° C. was treated with EDCI (1.99 g, 10.40 mmol) and stirred 14 h with ice bath expiring. The reaction mixture was diluted with CH₂Cl₂ (50 mL) and H₂O (50 mL) and layers separated. The aqueous layer was extracted with CH₂Cl₂ (3×50 mL). The combined organic layers were washed with H₂O (50 mL), brine (50 mL), dried over MgSO₄, and concentrated in vacuo to afford a black foamy solid. Purification via Biotage chromatography (eluting with 2% MeOH(NH₃)/CH₂Cl₂) gave 121 (1.76 g) as a pale red solid in 76% yield; ¹H NMR (400 MHz, DMSO-d₆) δ 8.18 (t, J=5.5 Hz, 1 H), 7.68 (d, J=8.7 Hz, 2 H), 7.52 (d, J=8.7 Hz, 2 H), 7.34 (d, J=8.7 Hz, 2 H), 6.56 (d, J=8.7 Hz, 2 H), 6.02 (s, 2 H), 4.72 (m, 1 H), 4.41 (d, J=7.9 Hz, 1 H), 4.20 (d,J=7.9 Hz, 1 H), 4.12 (t, J=9.0 Hz, 1 H), 4.01 (d, J=9.0 Hz, 1 H), Hz, 1 H), 4.20 (d, J=7.9 Hz, 1 H), 4.12 (t, J=9.0 Hz, 1 H), 4.01 (d, J=9.0 Hz, 1 H), 3.85 (d, J=9.0 Hz, 1 H), 3.76 (dd, J=9.0, 6.4 Hz, 1 H), 3.42 (m, 2 H), 3.07 (t, J=6.4 Hz, 2 H), 2.37 (t, J=6.0 Hz, 2 H), 2.10 (q, J=7.7 Hz, 2 H), 1.57 (s, 3 H), 0.96 (t, J=7.5 Hz, 3 H); ¹³C NMR (100 MHz, DMSO-d₆) δ 195.57, 173.66, 172.10, 154.05, 47.12, 41.25, 37.01, 31.77, 28.84, 28.26, 24.84, 9.83.

Example 37 N-({(5S)-3-[4-(1-{4-[4-(glycylamino)phenyl]-4-oxobutanoyl}-3-methylazetidin-3-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)propanamide

[0371]

[0372] A solution of 121 (from Example 36)(1.00 g, 2.03 mmol) and FmocGlyCl (770 mg, 2.44 mmol) in CH₂Cl₂ (15 mL) at rt was treated with pyridine (0.82 mL, 10.15 mmol) and let stir for 90 min. The reaction was then diluted with CH₂Cl₂ (200 mL), washed with H₂O (75 mL), 0.1 M HCl (75 mL), brine (50 mL), dried over MgSO₄, and chromatography (eluting with 5% MeOH/CH₂CI₂) affords the Fmoc-protected chromatography (eluting with 5% MeOH/CH₂Cl₂) affords the Fmoc-protected subsequently treated with piperidine (0.19 mL) in DMF (5.0 mL) at rt for 20 min, and subsequently treated with piperidine (0.19 mL) in DMF (5.0 mL) at rt for 20 min, and with 5-10% MeOH/CH₂Cl₂ and then with 10% MeOH(NH₃)/CH₂Cl₂) followed by trituration (Et₂O) affords 122 (258 mg) as a pale grey solid; ¹H NMR (400 MHz, trituration (Et₂O) affords 122 (258 mg) as a pale grey solid; ¹H NMR (400 MHz, DMSO-d₆) δ 8.19 (t, J=5.7 Hz, 1 H), 7.95 (d, J=8.7 Hz, 2 H), 7.78 (d, J=8.7 Hz, 2 H), 7.53 (d, J=8.7 Hz, 2 H), 7.35 (d, J=8.7 Hz, 2 H), 4.73 (m, 1 H), 4.42 (d, J=8.1 Hz, 1 H), 4.22 (d, J=8.1 Hz, 1 H), 4.13 (t, J=9.1 Hz, 1 H), 4.03 (d, J=9.1 Hz, 1 H), 3.86 (d, J=9.3 Hz, 1 H), 3.76 (dd, J=9.0, 6.3 Hz, 1 H), 3.43 (m, 3 H), 3.31 (s, 2 H), 3.21 (t, J=6.2 Hz, 2 H), 2.43 (t, J=5.6 Hz, 2 H), 2.11 (q, J=7.7 Hz, 2H), 1.58 (s, 3 H), 0.96 (t, J=7.6 Hz, 3 H); ¹³C NMR (100 MHz, DMSO-d₆) δ 197.19, 173.67, 117.99, 71.45, 61.84, 59.80, 54.81, 47.12, 45.55, 41.25, 37.07, 32.43, 28.86, 28.26, 24.69, 9.83.

Example 38 N-{[(5S)-3-(4-{1-[4-(4-aminophenyl)-4-oxobutanoyl]-3-methylazetidin-3-yl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide

[0373]

[0374] A solution of 123 (Prepared as described in U.S. Pat. No. 5,968,962, 1.50 g, 3.34 mmol), 4-(4-aminophenyl)-4-oxobutanoic acid (645 mg, 3.34 mmol), and Hunig's base (2.91 mL, 16.69 mmol) in CH₃CN (56 mL) at 0° C. was treated dropwise with a solution of HATU (1.33 g, 3.51 mmol) in CH₃CN (38 mL). Additional Hunig's base was stirred 14 h with ice bath expiring. The reaction mixture was concentrated in vacuo, and residue was dissolved in CH₂Cl₂. This organic layer was washed initially with 1.0 M HCl; however, back-extraction with CH₂Cl₂ was necessary to retrieve much of the desired product from the aqueous layer. The organic layers are combined, washed with brine, dried over MgSO₄, and concentrated in vacuo. Purification via Biotage chromatography (eluting with 4% MeOH/CH₂Cl₂) affords 124 (1.42 g) as a red solid in 86% yield; ¹H NMR (400 MHz, DMSO-d₆) δ 8.25 (t, J=5.8 Hz, 1 H), 7.67 (d, J=8.5 Hz, 2 H), 7.50 (dd, J=13.5, 1.7 Hz, 1 H), 7.31 (m, 2 H), 6.55 (d, J=8.7 Hz, 2 H), 6.02 (s, 2 H), 4.74 (m, 1 H), 4.48 (d, J=8.1 Hz, 1 H), 4.21 (d, J=8.3 Hz, 1 H), 4.12 (m, 2 H), 3.85 (d, J=9.3 Hz, 1 H), 3.74 (dd, J=9.1, 6.4 Hz, 1 H), 3.42 (t, J=5.5 Hz, 2 H), 3.06 (t, J=6.4 Hz, 2 H), 2.36 (m, 2 H), 1.84 (s, 3 H), 1.56 (s, 3 H); ¹³C NMR (100 MHz, DMSO-d₆) δ 195.52, 172.19, 169.88, 161.26, 158.05, 153.88, 153.46, 138.57, 138.43, 130.07, 127.82, 127.74, 127.63, 127.43, 124.15, 113.41, 112.32, 105.66, 105.30, 71.58, 60.77, 58.62, 54.81, 47.07, 41.25, 35.07, 31.73, 28.02, 24.84, 22.34.

Example 39 N˜1˜-(4-{4-[3-(4-{(5S)-5-[(acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-3-methylazetidin-1-yl]-4-oxobutanoyl}phenyl)glycinamide (125).

[0375]

[0376] A solution of 124 (from Example 38) (790 mg, 1.59 mmol) and CbzGlyOH (349 mg, 1.67 mmol) in CH₃CN (40 mL) at 0° C. was treated with Hunig's base (1.39 mL, 7.96 mmol) followed by HATU (635 mg, 1.67 mmol) and stirred 14 h with ice bath expiring. The reaction mixture was concentrated in vacuo, and the residue dissolved in CH₂Cl₂ (200 mL). This organic phase was washed with 1.0 M HCl, saturated aqueous NaHCO₃, brine, dried over MgSO₄, and concentrated in vacuo. Purification via Biotage chromatography (eluting with 5% MeOH/CH₂Cl₂) affords the Cbz-protected amine (313 mg) as a pale yellow solid in 29% yield. This compound was subsequently placed under N₂ (g) in 10:1 THF:MeOH (11 mL) and treated with Pd/C (80 mg). The reaction vessel was then charged with H₂ (g) and the reaction mixture was stirred for 2 d at rt. After filtering to remove Pd/C, the filtrate was concentrated in vacuo. Purification via Biotage chromatography (eluting with 4% MeOH(NH₃)/CH₂Cl₂) affords 125 (99 mg) as a pale yellow-green solid: ¹H NMR (400 MHz, DMSO-d₆) δ 8.26 (t, J=5.8 Hz, 1 H), 7.94 (d, J=8.9 Hz, 2 H), 7.77 (d, J=8.7 Hz, 2 H), 7.50 (dd, J=13.6, 1.6 Hz, 1 H), 7.31 (m, 2 H), 4.74 (m, 1 H), 4.49 (d, J=8.1 Hz, 1 H), 4.22 (d, J=8.1 Hz, 1 H), 4.13 (m, 2 H), 3.86 (d, J=9.3 Hz, 1 H), 3.74 (dd, J=9.0, 6.5 Hz, 1 H), 3.42 (t, J=5.4 Hz, 2 H), 3.32 (s, 2 H), 3.20 (t, J=6.3 Hz, 2 H), 2.42 (m, 2 H), 1.84 (s, 3 H), 1.57 (s, 3 H); ¹³C NMR (100 MHz, DMSO-d₆) δ 197.15, 172.49, 171.89, 169.89, 161.28, 158.06, 153.89, 142.99, 138.59, 138.45, 131.11, 129.07, 127.83, 127.71, 127.60, 127.42, 118.13, 113.42, 105.67, 105.31, 71.59, 60.81, 58.69, 48.48, 47.08, 45.47, 41.26, 35.14, 32.41, 28.03, 24.71, 22.34.

Example 40 Preparation of 2-[3-(4-{(5S)-5-[(acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-3-methylazetidin-1-yl]-2-oxoethyl-4-(aminoethyl)benzamide (126).

[0377]

[0378] A solution of N-(4-{[(tert-butoxycarbonyl)amino]methyl}benzoyl)glycine (216 mg, 0.70 mmol) and Hunig's base (0.23 mL, 1.34 mmol) in CH₃CN (10 mL) at 0° C. was treated with HATU (266 mg, 0.70 mmol) and let stir for 35 min. A solution of 123 (300 mg, 0.67 mmol) in CH₃CN/DMF (5 mL/1 mL) was added along with more Hunig's base (0.35 mL, 2.00 mmol). The reaction was stirred for 30 min with ice bath expiring, then concentrated in vavuo, and the amber residue was dissolved in CH₂Cl₂ (100 mL), washed with 0.1 M HCl (2×30 mL), saturated aqueous NaHCO₃ (40 mL), brine (40 mL), dried over MgSO₄, and concentrated in vacuo to afford a yellow-brown solid. Purification via Biotage chromatography (eluting with 4-5% MeOH/CH₂Cl₂) affords the Boc-protected amine (300 mg) as a white solid in 74% yield. This compound (750 mg) was treated with TFA (3.0 mL) in CH₂Cl₂ (10 mL) at 0° C. for 20 min, and then stirred an additional 50 min at rt. Concentration in vacuo followed by purification via Biotage chromatography (eluting first with 5% MeOH/CH₂Cl₂ and then with 5% MeOH(NH₃)/CH₂Cl₂) and trituration (Et₂O) affords 126 (463 mg) as a white solid; ¹H NMR (400 MHz, DMSO-d₆) δ 8.65 (t, J=5.6 Hz, 1 H), 8.26 (t, J=5.8 Hz, 1 H), 7.81 (d, J=8.1 Hz, 2 H), 7.51 (dd, J=13.7, 1.9 Hz, 1 H), 7.42 (d, J=8.3 Hz, 2 H), 7.31 (m, 2 H), 4.74 (m, 1 H), 4.52 (d, J=8.3 Hz, 1 H), 4.26 (d, J=8.5 Hz, 1 H), 4.18 (d, J=9.5 Hz, 1 H), 4.12 (t, J=9.0 Hz, 1 H), 3.88 (m, 3 H), 3.76 (s, 2 H), 3.74 (dd, J=9.0, 6.4 Hz, 1 H), 3.42 (t, J=5.4 Hz, 2 H), 1.84 (s, 3 H), 1.57 (s, 3 H); ¹³C NMR (100 MHz, DMSO-d₆) δ 169.89, 169.08, 166.12, 161.24, 158.02, 153.89, 147.67, 138.64, 138.49, 131.64, 127.78, 127.69, 127.44, 127.26, 126.98, 126.66, 113.46, 105.67, 105.31, 71.60, 60.91, 59.01, 48.48, 47.08, 45.18, 41.26, 35.72, 27.97, 22.34.

Example 41 N-{[(5S)-3-(3-Fluoro-4-{4-[4-(4-methoxyphenyl)butanoyl]piperazine-1-yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide (127). 34709-SCP-137.

[0379]

[0380] A stirred mixture of 4-(4-methoxyphenyl)butanoic acid (0.41 g, 2.11 mmol) in pyridine (10 ml), under nitrogen, was treated with EDC (0.48 g, 2.5 mmol), 3 PNU-99388 (0.78 g, 2.1 mmol) and DMAP (10 mg), kept at ambient temperature for 22 h and concentrated in vacuo. A mixture of the residue and 5% NaHCO₃ was extracted with EtOAc. The extract was washed with water and brine, dried (MgSO₄) and concentrated. Crystallization of the residue from EtOAc gave 0.75 g of 4: mp 164-165° C.; IR (drift) 3307, 1730, 1654, 1630 cm⁻¹. Anal. calcd for C₂₇H₃₃FN₄O₅: C, 63.27; H, 6.49; N, 10.93. Found: C, 63.20; H, 6.60; N, 10.95.

Example 42 N-{[(5S)-3-(3-Fluoro-4-{4-[4-(4-hydroxyphenyl)butanoyl]piperazin-1-yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide (128).

[0381]

[0382] An ice cold, stirred suspension of 127 (0.25 g, 0.488 mmol) in CH₂Cl₂ (10 ml), under nitrogen, was treated, dropwise during 2 min, with a 1 M solution of boron tribromide in CH₂Cl₂ (1.02 ml). It was warmed to ambient temperature during 2 h, stirred at 0° C. for 72 h, warmed to ambient temperature for 4.5 h and mixed with ice water (20 ml). A solution of the resulting gum in CH₂Cl₂ was concentrated and the residue was chromatographed on silica gel with 7% MeOH—CH₂Cl₂. Crystallization of the product from MeOH gave 0.104 g of 128: mp 119-120° C. (dec); ¹H NMR [400 MHz, (CD₃)₂SO] δ 1.76 (m, 2H), 1.83 (s, 3H), 2.32 (t, 2H), 2.48 (m, 2H), 2.92 (m, 4H), 3.17 (s, 3H, MeOH), 3.40 (t, 2H), 3.57 (m, 4H), 3.69 (dd, 1H), 4.08 (t, 1H), 4.08 (broad s, 1H), 4.70 (m, 1H), 6.67 (d, 2H), 6.98 (d, 2H), 7.07 (t, 1H), 7.17 (dd, 1H), 7.49 (dd, 1H), 8.25 (t, 1H), 9.13 (s, 1H); MS (ESI+) m/z 499.4 (M+H⁺), 521 (M+Na⁺); MS (ESI−) m/z 497.3 (M−H), 533.3 (M+Cl), 577, 579.2, (M+Br); IR (drift) 3273, 3269, 1731, 1643, 1638, cm⁻¹. Anal. calcd for C₂₆H₃₁FN₄O₅.CH₃OH: C, 61.12; H, 6.65; N, 10.56. Found: C, 60.94; H, 6.64; N, 10.56.

Example 43 2,2-Difluoro-N-{[(5S)-3-(3-fluoro-4-{4-[4-(4-methoxyphenyl)butyanoyl]piperazin-1-yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}ethanethioamide (129).

[0383] Step 1:

[0384] A stirred mixture of 4-(4-methoxyphenyl)butanoic acid (0.8 g, 4.1 mmol) and pyridine (20 ml), under nitrogen was treated with EDC (0.96 g, 5.0 mmol), 17a (1.69 g, 4.28 mmol) and DMAP (20 mg) and kept at ambient temperature for 22 h. It was concentrated in vacuo and the residue was mixed with 5% aqueous NaHCO₃ and extracted with Et₂O. The extract was washed with water and brine, dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with 2% MeOH—CH₂Cl₂ and crystallization of the product from EtOAc gave 1.26 g of 130: mp 140-141° C.; MS (ESI+) m/z 571.5 (M+H⁺), 593.5 (M+Na⁺); MS (ESI−) m/z 569.4 (M−H), 605 (M+Cl).

[0385] Step 2:

[0386] Compound 130 (0.5 g, 0.88 mmol) was cooled, under nitrogen, in an ice bath and treated, dropwise with stirring during 3 min with 4N HCl in dioxane (7 ml). It was kept in the ice bath for 45 min and at ambient temperature for 90 min. Excess hydrogen chloride was removed under a stream of nitrogen and the mixture was concentrated in vacuo to give 131, a white solid.

[0387] Step 3:

[0388] A stirred mixture of 131 (0.19 g) and CH₂Cl₂ (10 ml), under nitrogen, was treated with triethylamine (0.11 ml) and then, dropwise, with a solution of 131a (0.15 g, 0.49 mmol) in CH₂Cl₂ (2 ml). It was kept at ambient temperature for 5 h 20 min and concentrated in vacuo. Chromatography of the residue on silica gel with 1.75% MeOH—CH₂Cl₂ and crystallization of the product from EtOAc-hexane gave 0.14 g of 129: mp 128-129° C.; ¹H NMR [400 MHz, (CD₃)₂SO] δ 1.77 (m, 2H), 2.34 (t, 2H), 2.54 (m, 2H), 2.92 (m, 4H), 3.56, 3.60 (m, m, 4H), 3.71 (s, 3H), 3.82 (dd, 1H), 3.96 (m, 2H), 4.16 (t, 1H), 5.01 (m, 1H), 6.37, 6.50, 6.64 (s, s, s, 1H), 6.85 (d, 2H), 7.10 (m, 3H), 7.18 (dd, 1H), 7.50 (dd, 1H), 11.18 (t, 1H); MS (ESI+) m/z 365.3 (M+H⁺); MS (ESI−) m/z 563.3 (M−H), 599 (M+Cl); IR (drift) 3274, 1744, 1633, 1617 cm⁻¹. Anal. calcd for C₂₇H₃₁F₃N₄O₄S: C, 57.44; H, 5.53; N, 9.92. Found: C, 57.02; H, 5.52; N, 9.83.

Example 44 N-{[(5S)-3-(4-{4-[4-(4-Bromophenyl)-4-oxobutanoyl]-1-piperazinyl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide (132).

[0389]

[0390] A stirred mixture of 3-(4-bromobenzoyl)propionic acid (0.186 g, 0.723 mmol) and pyridine (6 ml), under nitrogen, was treated with EDC (0.13 g, 0.68 mmol), DMAP (10 mg) and 17b¹² (0.24 g, 0.72 mmol), kept at ambient temperature for 18 h and concentrated in vacuo. Chromatography of the residue on silica gel with 3% MeOH—CHCl₃ and crystallization of the product from CH₃CN gave 0.17 g of 132: mp 197-198° C.; MS (ESI+) mn/z 597, 599 (M+Na⁺); MS (ESI−) m/z 573, 575 (M−H), 609.2, 611.2 (M+Cl); IR (drift) 3311, 1742, 1687, 1647 cm⁻¹. Anal. calcd for C₂₆H₂₈BrFN₄O₅: C, 54.27; H, 4.90; N, 9.74. Found: C, 54.29; H, 4.97; N, 9.75.

Example 45 N-{[(5S)-3-(4-{4-[4-(4-Bromophenyl)-4-oxobutanoyl]-1-piperazinyl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}ethanethioamide (133).

[0391]

[0392] A stirred mixture 3-(4-bromobenzoyl)propionic acid (0.186 g, 0.723 mmol) and pyridine (6 ml), under nitrogen, was treated with EDC (0.13 g, 0.68 mmol), DMAP (10 mg) and 17c⁶ (0.25 g, 0.71 mmol), kept at ambient temperature for 18 h and concentrated in vacuo. Chromatography of the residue on silica gel with 3% MeOH—CHCl₃ and crystallization of the product from CH₃CN gave 0.23 g of 133: mp 219-220° C. (dec); MS (ESI+) m/z 613, 615 (M+Na⁺); MS (ESI−) m/z 589, 591 (M−H), 625.2, 627.2 (M+Cl); IR (drift) 3238, 1755, 1680, 1645, 1620 cm⁻¹. Anal. calcd for C₂₆H₂₈BrFN₄O₄S: C, 52.79; H, 4.77; N, 9.47. Found: C, 52.82; H, 4.86; N, 9.86.

Example 46 N-{[(5S)-3-(4-{4-[4-(4-Cyanophenyl)-4-oxobutanoyl]-1-piperazinyl}-3-fluorophenyl-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide (135).

[0393] Step 1:

[0394] According to the method of Curran and Ross⁸ a stirred mixture of 3-(4-bromobenzoyl)propionic acid (4.57 g, 0.0178 mol), copper (I) cyanide (1.84 g, 0.0205 mol) and DMF (12 ml) was refluxed, under nitrogen, for 4 h, cooled for 5 min, combined with a mixture of water (12 ml), FeCl₃.6 H₂O (7.8 g) and concentrated HCl (1 ml) and warmed on the steam bath for 20 min. This mixture was poured into water (100 ml) and cooled in an ice bath. The solid was collected by filtration, washed with cold water, and dried in vacuo. A portion of this material was chromatographed on silica gel with 2.5% MeOH-0.25% HOAc-CH₂Cl₂ to give 0.7 g of 134: MS (ESI−) m/z 201.9 (M−H). The remaining product was crystallized from CHCl₃ to give 1.23 g of additional 134.

[0395] Step 2:

[0396] A stirred mixture of 3-(4-cyanobenzoyl)propionic acid 134 (0.178 g, 0.88 mmol) and pyridine (6 ml), under nitrogen was treated with EDC (0.16 g, 0.83 mmol) and 4-dimethylaminopyridine (10 mg), kept at ambient temperature for 5 min, treated with 61¹² (0.29 g, 0.862 mmol) and kept at ambient temperature for 3 h and at 10° C. for 18 h. It was concentrated in vacuo and the residue was chromatographed on silica gel with 2-5% MeOH—CH₂Cl₂. Crystallization of the product from CH₃CN gave 0.261 g of 135: mp 197-198° C.; MS (ESI+) m/z 522.2 (M+H⁺), 544 (M+Na⁺); MS (ESI−) m/z 520.1 (M−H), 556.0 (M+Cl); IR (drift) 3296, 2234, 1757, 1693, 1640 cm⁻¹; ¹H NMR [300 MHz, (CD₃)₂SO]δ 1.81 (s, 3H), 2.06 (s, 1.4H, CH₃CN), 2.77 (t, 2H), 2.89, 2.99 (s, s, 4H), 3.25 (t, 2H), 3.38 (t, 2H), 3.57 (s, 2H), 3.66 (m, 3H), 4.07 (t, 1H), 4.68 (m, 1H), 7.07 (t, 1H), 7.17 (dd, 1H), 7.49 (dd, 1H), 8.00 (d, 2H), 8.11 (d, 2H), 8.23 (t, 1H); HRMS (FAB) calcd for C₂₇H₂₉FN₅O₅ (M+H⁺) 522.2153, found 522.2139. Anal. calcd for C₂₇H₂₈FN₅O₅.0.5 CH₃CN: C, 62.04; H, 5.48; N, 14.21. Found: C, 61.31; H, 5.57; N, 13.95.

Example 47 4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}benzamide (137).

[0397] Step 1:

[0398] A mixture of boron trifluoride-acetic acid complex (0.74 ml, 5.3 mmol) and water (0.09 ml, 5.0 mmol) was added, under nitrogen with stirring to 134 (0.20 g, 0.98 mmol) and the resulting mixture was warmed in an oil bath at 130° C. for 10 min, kept at ambient temperature for 1 h and rewarmed at 130° C. for 5 min. It was then concentrated under a stream of nitrogen. The residue was mixed with CH₂Cl₂ and MeOH to give 0.17 g of 136, a white solid: MS (ESI+) m/z 221.9 (M+H⁺), 244.0 (M+Na⁺); MS (ESI−) m/z 220 (M−H).

[0399] Step 2:

[0400] A stirred mixture of 136 (0.16 g, 0.72 mmol) and pyridine (6 ml) under nitrogen was treated with EDC (0.13 g, 0.68 mmol), DMAP (10 mg) and 17b¹² (0.24 g, 0.71 mmol) and kept at ambient temperature for 20 h. It was then concentrated in vacuo and the residue was chromatographed on silica gel with 7-10% MeOH—CH₂Cl₂. Crystallization of the product from MeOH—CH₂Cl₂ gave 0.219 g of 137: mp>250° C.; IR (drift) 3394, 3335, 3199, 1746, 1727, 1697, 1676, 1630 cm⁻¹. Anal. calcd for C₂₇H₃₀FN₅O₆: C, 60.10; H, 5.60; N, 12.98. Found: C, 59.60, 59.78; H, 5.64, 5.64; N, 12.77, 12.91.

Example 48 4-{4-[4-(4-{(5S)-5-[(Ethanethiolylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}benzamide 138.

[0401]

[0402] A stirred mixture of 136 (0.16 g, 0.72 mmol) in pyridine (6 ml) under nitrogen, was treated with EDC (0.13 g, 0.68 mmol) and DMAP (10 mg), kept at ambient temperature for 5 min and treated with 17c⁶ (0.25 g, 0.71 mmol). It was kept at ambient temperature for 2.5 h and concentrated in vacuo. Chromatography of the residue on silica gel with 6% MeOH—CH₂Cl₂ and crystallization of the product from CH₃CN gave 0.11 g, mp 219-220° C. (dec) and 0.13 g, mp 223-224° C. (dec) of 138: IR (drift) 3374, 3301, 3290, 3253, 3195, 1738, 1679, 1661, 1620 cm⁻¹. Anal. calcd for C₂₇H₃₀FN₅O₅S: C, 58.37; H, 5.44; N, 12.60. Found: C, 58.22; H, 5.46; N, 12.70.

Example 49 N-{[(5S)-3-(4-{4-[4-(4-Chlorophenyl)-4-oxobutanoyl]-1-piperazinyl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide 139.

[0403]

[0404] A stirred mixture of 3-(4-chlorobenzoyl)propionic acid (0.153 g, 0.72 mmol) in pyridine (6 ml), under nitrogen, was treated with EDC (0.14 g, 0.73 mmol), DMAP (10 mg) and 17b¹² (0.24 g, 0.72 mmol), kept at ambient temperature for 20 h and concentrated in vacuo. Chromatography of the residue on silica gel with 5% MeOH—CHCl₃ and crystallization of the product from CH₃CN gave 0.256 g of 139: mp 208-209° C.; IR (drift) 3328, 1741, 1672, 1645, 1625 cm⁻¹. Anal. calcd for C₂₆H₂₈ClFN₄O₅: C, 58.81; H, 5.32; N, 10.55. Found: C, 58.78; H, 5.36; N, 10.54.

Example 50 N-{[(5S)-3-(4-{4-[4-(4-chlorophenyl)-4-oxobutanoyl]-1-piperazinyl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}ethanethioamide 140.

[0405]

[0406] A stirred mixture of 3-(4-chlorobenzoyl)propionic acid (0.153 g, 0.720 mmol) in pyridine (6 ml), under nitrogen was treated with EDC (0.13 g, 0.68 mmol), DMAP (10 mg) and 17c⁶ (0.25 g, 0.71 mmol), kept at ambient temperature for 20 h and concentrated in vacuo. Chromatography of the residue on silica gel with 2% MeOH—CH₂Cl₂ and crystallization of the product from CH₃CN gave 0.226 g of 140: mp 215-216° C. (dec); IR (drift) 3235, 1755, 1679, 1620 cm⁻¹. Anal. calcd for C₂₆H₂₈ClFN₄O₄S: C, 57.08; H, 5.16; N, 10.24. Found: C, 57.09; H, 5.24; N, 10.43.

Example 51 N-[((5S)-3-{3-Fluoro-4-[4-(4-{4-[(methylsulfonyl)amino]phenyl}-4-oxobutanoyl)-1-piperazinyl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide 141.

[0407] Step 1:

[0408] A stirred mixture of PNU-68849 4-[(methylsulfonyl)amino]-□-oxo-Benzenebutanoic acid, (0.583 g, 2.15 mmol) and triethylamine (0.35 ml) in THF (20 ml), under nitrogen, was cooled in an ice-MeOH bath and treated, dropwise with isobutyl chloroformate (0.33 ml). It was kept in the bath for 30 min and then treated with a mixture of 17a⁵ (0.85 g, 2.15 mmol), triethylamine (0.35 ml) and THF (15 ml). This mixture was kept at 0° C. for 90 min and concentrated in vacuo. Chromatography of the residue on silica gel with 2% MeOH—CH₂Cl₂ and crystallization of the product from CH₃CN gave 0.64 g, mp 171-173° C. (dec) and 0.151 g, mp 173-175° C. (dec) of 142: MS (ESI) 670.3 (M+Na⁺).

[0409] Step 2:

[0410] A stirred solution of 142 (0.42 g, 0.65 mmol) in dioxane (8 ml) was cooled in an ice bath and treated, dropwise during 4 min, with ice cold 4N HCl in dioxane (6 ml). The mixture was kept in the ice bath for 1 h, at ambient temperature for 3 h and at 4° C. for 18 h. It was then concentrated in vacuo to give 0.4 g of 143: MS (ESI) m/z 548.2 (M+H⁺).

[0411] Step 3:

[0412] A stirred mixture of 143 (0.16 g), triethylamine (0.15 ml, 1.08 mmol) and MeOH (10 ml), under nitrogen, was treated with ethyl dithiopropionate (0.05 ml, 0.39 mmol), kept at ambient temperature for 3 h and concentrated in vacuo. The residue was found to be a mixture of starting material and product. It was mixed with MeOH (6 ml), triethylamine (0.1 ml) and ethyl dithiopropionate (0.04 ml) and stirred at ambient temperature for 6 h. This mixture was concentrated and the residue was chromatographed on silica gel with 2% MeOH—CH₂Cl₂. Crystallization of the product from MeOH gave 0.07 g of 141: mp 201-202° C. (dec) with softening at 198° C.; ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.13 (t, 3H), 2.57 (q, 2H), 2.71 (t, 2H), 2.90, 3.00 (s, s, 4H), 3.09 (s, 3H), 3.18 (t, 2H), 3.57, 3.64 (s, s, 4H), 3.78 (dd, 1H), 3.90 (t, 2H), 4.12 (t, 1H), 4.92 (m, 1H), 7.08 (t, 1H), 7.17 (dd, 1H), 7.28 (d, 2H), 7.50 (dd, 1H), 7.95 (d, 2H), 10.31 (s, 1H); MS (ESI) m/z 642.2 (M+Na⁺); HRMS (FAB) calcd for C₂₈H₃₅FN₅O₆S₂ (M+H⁺) 620.2012, found 620.2006; IR (drift) 3301, 3177, 3159, 1747, 1674, 1630 cm⁻¹.

Example 52 N-[((5S)-3-{3-Fluoro-4-[4-(4-{4-[(methylsulfonyl)amino]phenyl}-4-oxobutanoyl-1-piperazinyl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide 144.

[0413]

[0414] A sample of 143 (prepared from 0.35 g, 0.54 mmol of 17a) was stirred with a mixture of Et₂O (5 ml) and 5% NaHCO₃ (10 ml) and concentrated under a stream of nitrogen. The resulting solid was collected by filtration, washed with water and dried to give 0.23 g of the free base. A stirred suspension of this material in pyridine (3 ml), under nitrogen, was cooled in an ice bath and treated with acetic anhydride (0.16 ml). It was kept in the ice bath for 1 h and at ambient temperature for 2.5 h and then concentrated in vacuo. The product was found to be a mixture of 144 and a compound in which both the amine and the sulfonamide nitrogen had been acetylated. A solution of the residue in MeOH was therefore hydrolyzed with 10% aqueous K₂CO₃ (2 ml). When the reaction was complete the mixture was concentrated and the residue was mixed with water, neutralized with 10% KHSO₄ and extracted with CH₂Cl₂. The extract was dried (Na₂SO₄) and concentrated. Chromatography of the residue on silica gel with 3-5% MeOH—CH₂Cl₂ and crystallization of the product from MeOH gave 0.102 g of 144: mp 220-222° C. (dec); MS (ESI) m/z 590.3 (M+H⁺), 612 (M+Na⁺); IR (drift) 3374, 3348, 3168, 3154, 1759, 1674, 1623, 1602 cm⁻¹; HRMS (FAB) calcd for C₂₇H₃₃FN₅O₇S (M+H⁺) 590.2084, found 590.2098. Anal. calcd for C₂₇H₃₂FN₅O₇S: C, 55.00; H, 5.47; N, 11.88. Found: C, 54.72; H, 5.55; N, 11.78.

Example 53 N-(4-{4-[4-(2-Fluoro-4-{(5S)-2-oxo-5-[(propanethiolylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)-1-piperazinyl]-4-oxobutanoyl}phenyl)acetamide 145.

[0415] Step 1:

[0416] Dimethylformamide (19.1 ml) was added, dropwise during 30 min, under nitrogen with stirring to aluminum chloride (116.5 g). The addition was exothermic and gave a semiliquid mass. This mixture was warmed in an oil bath at 70° C. and treated, portionwise during 10 min, with a mixture of acetanilide (12.5 g, 0.0925 mol) and succinic anhydride (8.35 g, 0.0834 mol). It was kept at 70-72° C. for 1 h and then poured into ice (800 g). The resulting solution was treated with a mixture of concentrated HCl (50 ml) and ice (50 g) to give a precipitate which was collected by filtration washed with cold water and dried. Crystallization of the solid from acetonitride gave 10.7 g of 146: MS (ESI) m/z 236.1 (M+H⁺), 258.1 (M+Na⁺).

[0417] Step 2:

[0418] A stirred mixture of 146 (1.01 g, 4.29 mmol) and triethylamine (0.69 ml, 4.96 mmol) in THF (20 ml), under nitrogen was cooled in an ice-MeOH bath and treated, dropwise with isobutyl chloroformate (0.66 ml, 5.1 mmol). It was kept in the bath for 30 min and then treated, in portions during 4 min, with a mixture of 17a⁵ (1.69 g, 4.28 mmol), triethylamine (0.69 ml, 4.96 mmol) and THF (15 ml). The mixture was allowed to warm to 10° C. during 2 h when it was concentrated in vacuo. A mixture of the residue and CH₂Cl₂ was washed with saturated NaHCO₃, water and brine, dried (Na₂SO₄) and concentrated. Chromatography of the residue on silica gel with 5% MeOH—CHCl₃ gave 1.84 g of 147: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.34 (s, 9H), 2.07 (s, 3H), 2.71 (t, 2H), 2.89, 2.99 (s, s, 4H), 3.18 (t, 2H), 3.25 (t, 2H), 3.57, 3.66 (s, s, 4H), 3.75 (dd, 1H), 4.06 (t, 1H), 4.66 (m, 1H), 7.07 (t, 1H), 7.18 (m, 2H), 7.48 (dd, 1H), 7.69 (d, 2H), 7.93 (d, 2H), 10.28 (s, 1H); MS (ESI) m/z 612.3 (M+H⁺), 634.2 (M+Na⁺).

[0419] Step 3:

[0420] A stirred mixture of 147 (1.0 g, 1.63 mmol) in dioxane (25 ml), under nitrogen was cooled in an ice bath and treated with ice-cold 4N hydrogen chloride in dioxane (10 ml). It was kept in the ice bath for 1.5 h, at ambient temperature for 4 h and at 0° C. for 14 h. It was then kept at ambient temperature for 2 h and concentrated in vacuo to give 1.04 g of 148, a white powder.

[0421] Step 4:

[0422] A stirred mixture of 148 (0.51 g), triethylamine (0.37 ml, 2.7 mmol) and MeOH (20 ml), under nitrogen, was treated with ethyl dithiopropionate (0.13 ml, 1.02 mmol), kept at ambient temperature for 4 h and concentrated under a stream of nitrogen for 1 h. The solid product was collected by filtration, and the filtrate was concentrated under a stream of nitrogen. Trituration of the residue with MeOH gave additional product. Chromatography of the combined product on silica gel with 2.5% MeOH—CH₂Cl₂ and crystallization from MeOH gave 0.326 g of 145: mp 198-199° C. (dec) with softening at 195° C.; MS (ESI) m/z 584.3 (M+H⁺), 606.3 (M+Na⁺); IR (drift) 3258, 3193, 1742, 1697, 1678, 1615 cm⁻¹. Anal. calcd for C₂₉H₃₄FN₅O₅S: C, 59.68; H, 5.87; N, 12.00. Found: C, 59.45; H, 5.94; N, 11.94.

Example 54 2-Amino-N-(4-{4-[4-(2-fluoro-4-{(5S)-2-oxo-5-[(propanethiolylamino)methyl]1,3-oxazolidin-3-yl}phenyl)-1-piperazinyl]-4-oxobutanoyl}phenyl)acetamide 149.

[0423] Step 1:

[0424] A mixture of 146 (4.97 g, 0.021 mol) and concentrated HCl (35 ml) was warmed on the steam bath for 20 min and the resulting solution was placed under a stream of nitrogen for 30 min. The resulting mixture was diluted with water (50 ml) and adjusted to pH 4 with solid Na₂CO₃. The solid product was collected by filtration, washed with water and dried in vacuo at 50° C. to give 3.95 g of 150 which could be recrystallized from acetonitrile. A second crop, 0.31 g of 150 was obtained from the aqueous filtrate.

[0425] Step 2:

[0426] A stirred mixture of 150 (0.47 g, 0.00243 mol), N-Fmoc-glycyl chloride (0.85 g, 0.0027 mol) and THF (50 ml) was refluxed, under nitrogen for 4 h and cooled to ambient temperature. The solid was collected by filtration to give 0.18 g of 151. Concentration of the mother liquor gave an additional 1.14 g of 151: MS (ESI+) m/z 495 (M+Na); MS (ESI−) m/z 471 (M−H).

[0427] Step 3:

[0428] An ice cold, stirred mixture of 151(0.17 g, 0.36 mmol) and DMF (3 ml), under nitrogen was treated with 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.08 g, 0.42 mmol) and 1-hydroxybenzotriazole hydrate (0.05 g, 0.37 mmol), kept for 20 min and then treated with 17a⁵ (0.14 g, 0.35 mmol) in portions during 10 min. The mixture was kept in the ice bath for 1 h 45 min and at ambient temperature for 45 min and then concentrated in vacuo. Chromatography of the semisolid residue on silica gel with 2% MeOH—CH₂Cl₂ gave 0.18 g of 152: MS (ESI−) m/z 883.2 (M+Cl); ¹H NMR (300 MHz, CDCl₃) δ 1.42 (s, 9H), 2.81 (m, 2H), 3.16 (s, s, 2H), 3.38 (m, 4H), 3.54 (m, 4H), 3.79 (m, 3H), 4.04 (m, 4H), 4.16 (s, 3H), 4.25 (t, 1H), 4.50 (d, 2H), 4.78 (m, 1H), 5.03 (m, 1H), 5.64 (m, 1H), 7.04 (m, 1H), 7.32 (m, 3H), 7.42 (m, 3H), 7.61 (m, 5H), 7.77 (m, 3H), 7.96 (m, 3H), 8.57 (m, 1H). Step 4:

[0429] A stirred suspension of 152 (0.34 g, 0.4 mmol) in dioxane (24 ml), under nitrogen was treated with ice cold 4N HCl in dioxane (6 ml) with cooling in an ice bath. It was kept in the ice bath for 1.25 h, at ambient temperature for 3 h, at 0° C. for 18 h and at ambient temperature for 6 h. It was then placed under a stream of nitrogen for 30 min and concentrated in vacuo to give 7153.

[0430] Step 5:

[0431] A stirred mixture of 153 from the previous reaction, ethyl dithiopropionate (0.073 ml) and triethylamine (0.22 ml) in MeOH (15 ml), under nitrogen, was kept at ambient temperature for 2 h, treated with additional MeOH (15 ml) and kept at ambient temperature for 21 h. The reaction was still not complete. The mixture was treated with additional triethylamine (0.1 ml) and kept for 24 h; it was then treated with additional ethyl dithiopropionate (0.07 ml) and kept at ambient temperature for 6 h and at 0° C. for 72 h. It was concentrated under a stream of nitrogen for 7 h and then in vacuo. Chromatography of the residue on silica gel with 1.5-3% MeOH—CH₂Cl₂ gave 0.09 g of 154: MS (ESI−) m/z 819 (M−H), 855 (M+Cl).

[0432] Step 6:

[0433] A stirred mixture of 154 (0.10 g, 0.12 mmol), “trisamine” resin (0.12 g, 0.48 mmol) and THF (10 ml) was refluxed, under nitrogen for 5 h, kept at ambient temperature for 18 h and refluxed for 4 h. It was filtered, the solid was washed with THF and MeOH and the filtrate was concentrated in vacuo. Chromatography of the residue over silica gel with 4% MeOH-0.25% NH₄OH—CH₂Cl₂ and crystallization of the product from MeOH-EtOAc gave 0.0516 g of 149, mp 197-198° C. (dec): MS (ESI+) m/z 599.3 (M+H⁺); MS (ESI−) m/z 633.0 (M+Cl−); IR (drift) 3283, 1736, 1680, 1644, 1630 cm⁻¹; HRMS (FAB) calcd for C₂₉H₃₆FN₆O₅S (M+H⁺) 599.2452, found 599.2471.

Example 55 N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}phenyl)-2-aminoacetamide 155.

[0434] Step 1:

[0435] A stirred mixture of 151 (0.19 g, 0.40 mmol), EDC (0.08 g, 0.42 mmol) and HOBT (0.05 g, 0.37 mmol) in DMF (3 ml), under nitrogen, was kept at ambient temperature for 30 min and treated with 17b¹² (0.12 g, 0.36 mmol). It was kept at ambient temperature for 18 h, treated with additional EDC (0.08 g) and HOBT (0.05 g), and kept at ambient temperature for 72 h. This mixture was concentrated in vacuo and the residue was chromatographed on silica gel with 2.5-4% MeOH—CH₂Cl₂ to give 0.06 g of 156: MS (ESI−) m/z 825.2 (M+Cl⁻); ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.81 (s, 3H), 2.71 (t, 2H), 2.90, 3.00 (s, s, 4H), 3.19 (t, 2H), 3.38 (t, 2H), 3.55 (s, 2H), 3.66 (m, 3H), 3.82 (d, 2H), 4.07 (t, 1H), 4.27 (m, 3H), 4.67 (m, 1H), 7.08 (t, 1H), 7.18 (dd, 1H), 7.40 (m, 6H), 7.70 (m, 5H), 7.95 (m, 4H), 8.21 (t, 1H).

[0436] Step 2:

[0437] A stirred mixture of 156 (0.15 g, 0.19 mmol) and CH₂Cl₂ (5 ml), under nitrogen was treated with piperidine (0.06 ml, 0.61 mmol) and kept at ambient temperature for 3.5 h. Additional piperidine (0.2 ml) was added and the mixture was kept at ambient temperature for 24 h and concentrated in vacuo. Chromatography of the residue on silica gel with 8% MeOH-0.5% NH₄OH—CH₂Cl₂ and crystallization of the product from MeOH-EtOAc gave 0.0459 g of 155: mp 221-222° C. (dec); MS (ESI+) m/z 569.3 (M+H⁺); MS (ESI−) m/z 603.2 (M+Cl⁻); IR (drift) 3322, 3297, 1742, 1687, 1645 cm⁻¹; ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.81 (s, 3H), 2.71 (t, 2H), 2.89, 2.99 (s, s, 4H), 3.19 (t, 2H), 3.30 (m, 5H), 3.38 (t, 2H), 3.57 (s, 2H), 3.66 (m, 3H), 4.07 (t, 1H), 4.69 (m, 1H), 7.07 (t, 1H), 7.16 (dd, 1H), 7.48 (dd, 1H), 7.77 (d, 2H), 7.95 (d, 2H), 8.23 (t, 1H); HRMS (FAB) calcd for C₂₈H₃₄FN₆O₆ (M+H⁺) 569.2524, found 569.2529.

Example 56 N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}phenyl)-(2S)-2-aminopropanamide 157.

[0438] Step 1:

[0439] A stirred mixture of 22 (0.50 g, 2.59 mmol) and (S)-N-Fmoc-alanyl chloride (0.939 g, 2.85 mmol) in THF (50 ml) was refluxed under nitrogen for 2 h, cooled and filtered. The filtrate was concentrated and the residue was crystallized from acetonitrile to give 0.78 g, mp 211-212° C. and 0.20 g, mp 210-211° C. of 24: MS (ESI+) m/z 309.2 (M+Na⁺); MS (ESI−) m/z 485.1 (M−H), 521.0 (M+Cl).

[0440] Step 2:

[0441] A mixture of 158 (0.35 g, 0.72 mmol), EDC (0.15 g, 0.78 mmol), HOBT (0.10 g, 0.74 mmol) and DMF (6 ml) was stirred under nitrogen for 15 min, treated with 17b¹² (0.24 g, 0.71 mmol) and kept at ambient temperature for 22 h. By TLC a considerable amount of 17b remained in the reaction mixture. It was treated with a mixture of 158 (0.175 g), EDC (0.075 g), HOBT (0.05 g) and DMF (2 ml) that had been prepared, under nitrogen, in a separate flask and stirred for 30 min. The resulting mixture was kept at ambient temperature for 72 h and concentrated in vacuo. Chromatography of the residue on silica gel with 3% MeOH—CH₂Cl₂ gave 0.14 g of 159: MS (ESI−) m/z 839.2 (M+Cl).

[0442] Step 3:

[0443] A stirred suspension of 159 (0.11 g, 0.14 mmol) in CH₂Cl₂ (20 ml), under nitrogen was treated with piperidine (0.3 ml) and kept at ambient temperature for 18 h. The resulting solution was concentrated in vacuo and the residue was chromatographed on silica gel with 4% MeOH-0.25% NH₄OH—CH₂Cl₂. A solution of the product in MeOH—CH₂Cl₂ was concentrated in vacuo to give 0.048 g of 157 as a foam: MS (ESI+) m/z 583.3 (M+H⁺); MS (ESI−) m/z 617.1 (M+Cl⁻); IR (drift) 3300, 1751, 1749, 1677, 1647 cm⁻¹; HRMS (FAB) calcd for C₂₉H₃₆FN₆O₆ (M+H⁺) 583.2680, found 583.2682.

Example 57 N-1-(4-{4-[4-(4-{(5S)-5-[(Ethanethiolylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}phenyl)-(S)-alaninamide 160.

[0444] Step 1:

[0445] A stirred mixture of 158 (0.213 g, 0.438 mmol) in DMF (2.5 ml), under nitrogen, was treated with EDC (0.084 g, 0.438 mmol) and HOBT (0.05 g, 0.375 mmol), kept at ambient temperature for 10 min and treated with 17c⁶ (0.123 g, 0.349 mmol). It was kept at ambient temperature for 18 h and concentrated in vacuo. Chromatography of the residue on silica gel with 3% MeOH—CH₂Cl₂ gave 0.29 g of 161: MS (ESI−) m/z 855.3 (M+Cl).

[0446] Step 2:

[0447] A stirred mixture of 161 (0.29 g, 0.35 mmol) and CH₂Cl₂ (45 ml), under nitrogen was treated with piperidine (0.8 ml) and kept at ambient temperature for 22 h. It was concentrated in vacuo and the residue was crystallized from CH₃CN. The solid was collected by filtration and the filtrate was concentrated. Chromatography of the residue on silica gel with 2.5% MeOH—CH₂Cl₂ and crystallization from CH₃CN gave 0.0675 g of 160: MS (ESI+) mn/z 599.4 (M+H⁺); MS (ESI−) m/z 597.4 (M−H), 633.3 (M+Cl); IR (drift) 3243, 3280, 3176, 1753, 1750, 1685, 1681, 1645, 1630 cm⁻¹; HRMS (FAB) calcd for C₂₉H₃₆FN₆O₅S (M+H⁺) 599.2452, found 599.2454.

Example 58 N¹-[4-(5-{4-[4-((5S)-5-{[(2,2-Difluoroethanethioyl)amino]methyl}-2-oxo-1,3-oxazolidin-3-yl)-2-fluorophenyl]piperazin-1-yl}-5-oxopentanoyl)phenyl]glycinamide 162.

[0448] Step 1:

[0449] Dimethylformamide (9.6 ml) was added, dropwise with stirring under nitrogen during 30 min to aluminum chloride (58.25 g) and the resulting mixture was warmed in a bath at 75° C. and treated, portionwise during 8 min, with a mixture of acetanilide (6.25 g, 0.0462 mol) and glutaric anhydride (4.75 g, 0.0417 mol). The mixture was kept at 72-75° C. for 1 h and then mixed with ice. The resulting stirred mixture was treated with a mixture of concentrated hydrochloric acid (25 ml) and ice (25 g). The product was collected by filtration, washed with cold water, dried and crystallized from acetonitrile to give 2.0 g of 163, mp 185-186° C. MS (ESI+) m/z 250.2 (M+H⁺), 272.2 (M+Na⁺), 288.1 (M+K⁺); MS (ESI−) m/z 248.1 (M−H), 284.1 (M+Cl).

[0450] Step 2:

[0451] A mixture of 163 (2.0 g, 8.0 mmol) and concentrated hydrochloric acid (10 ml) was warmed on the steam bath for 20 min and cooled under a stream of nitrogen for 20 min. It was then diluted with water (20 ml) and adjusted to pH 5 with solid Na₂CO₃. The mixture was cooled and the solid product was collected by filtration, washed with cold water and dried in vacuo to give 164: MS (ESI+) m/z 208.1 (M+H), 230.2 (M+Na⁺); MS (ESI−) m/z 206.1 (M−H), 242.1 (M+Cl).

[0452] Step 3:

[0453] A stirred mixture of 23 (0.50 g, 2.4 mmol) and N-Fmoc-glycyl chloride (0.85 g, 2.7 mmol) in THF (50 ml) was refluxed, under nitrogen, for 4 h, cooled and diluted with CH₂Cl₂ (50 ml). The white precipitate was collected by filtration to give 0.93 g of 25: mp 217-218° C.; MS (ESI−) m/z 485.2 (M−H), 521.2 (M+35). The filtrate was concentrated and the residue was mixed with Et₂O and filtered to give 0.20 g of additional 83, mp 215-216° C.

[0454] Step 4:

[0455] A stirred mixture of 165 (0.486 g, 0.999 mmol), 17a (0.4 g, 1.0 mmol) and pyridine (7 ml), under nitrogen, was treated with EDC (0.25 g, 1.3 mmol) and DMAP (10 mg) and kept at ambient temperature for 24 h. It was concentrated in vacuo and the residue was stored under a stream of nitrogen for 2 d. During this period it appeared (MS) that a considerable amount of the Fmoc protecting group had been removed. The residue was mixed with water and extracted with CH₂Cl₂. The extract was washed with water and brine, dried (Na₂SO₄) and concentrated to give 0.45 g of a mixture of 166 and the Fmoc deprotected material. A stirred mixture of this material in THF (20 ml), under nitrogen, was treated with diisopropylethylamine (0.13 ml, 0.77 mmol) and Fmoc chloride (0.14 g, 0.54 mmol) and kept at ambient temperature for 2.5 h. It was concentrated in vacuo and the residue was chromatographed on silica gel with 4% MeOH—CH₂Cl₂ to give 0.39 g of 166: MS (ESI+) m/z 863.5 (M+H⁺), 885.5 (M+Na⁺); MS (ESI−) m/z 897.5 (M+Cl).

[0456] Step 5:

[0457] The product 166 from the previous reaction was cooled in an ice bath, under nitrogen, and, with stirring, treated dropwise during 1.5 min with 4N HCl in dioxane (3 ml). It was kept in the ice bath for 45 min and at ambient temperature for 130 min. Excess hydrogen chloride was then removed under a stream of nitrogen and the resulting mixture was concentrated in vacuo to give 0.30 g of 167.

[0458] Step 6:

[0459] A stirred mixture of 167 (0.30 g) from the previous reaction in CH₂Cl₂ (25 ml), under nitrogen, was treated with triethylamine (0.11 ml) and then dropwise with a solution of O-(3,3-diphenylpropyl) difluoroethanethioate (0.15 g, 0.49 mmol) in CH₂Cl₂ (2 ml). It was kept at ambient temperature and treated with additional portions of O-(3,3-diphenylpropyl) difluoroethanethioate (0.05 g in 1 ml of CH₂Cl₂) after 2 h and 4 h. The resulting mixture was kept at ambient temperature for 18 h and concentrated in vacuo. The residue was triturated with 3% MeOH—CH₂Cl₂ and the resulting solid was crystallized from CH₂Cl₂-Et₂O to give 0.29 g of 168: MS (ESI+) m/z 879.6 (M+Na⁺); MS (ESI−) m/z 855.3 (M−H), 891.2 (M+Cl).

[0460] Step 7:

[0461] A stirred mixture of 168 (0.29 g) from the previous reaction in DMF (2 ml), under nitrogen, was treated dropwise with piperidine (0.07 ml), kept at ambient temperature for 30 min and concentrated in vacuo. Chromatography of the residue on silica gel with 4% MeOH-0.2% NH₄OH—CH₂Cl₂ and crystallization of the product from MeOH gave 0.08 g of 162: mp 196-197° C. (dec); ¹H NMR [400 MHz, (CD₃)₂SO] δ 1.85 (m, 2H), 2.43 (t, 2H), 292, 2.96 (m, m, 4H), 3.03 (t, 2H), 3.35 (s, 3H), 3.60 (m, 4H), 3.83 (dd, 1H), 3.94 (m, 2H), 4.15 (t, 1H), 5.00 (m, 1H), 6.32, 6.46, 6.59 (s, s, s, 1H), 7.07 (t, 1H), 7.19 (dd, 1H), 7.51 (d, 1H), 7.77 (d, 2H), 7.95 (d, 2H); MS (ESI+) m/z 635.4 (M+H⁺); MS (ESI−) m/z 633.3 (M−H), 669.3 (M+Cl); IR (drift) 3394, 3258, 1743, 1693, 1672, 1645 cm⁻¹. Anal. calcd for C₂₉H₃₃F₃N₆O₅S; C, 54.88; H, 5.24; N, 13.24. Found: C, 54.46; H, 5.27; N, 13.09.

Example 59 N¹-(4-{5-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-5-oxopentanoyl}phenyl)glycinamide 169.

[0462] Step 1:

[0463] A stirred mixture of 165 (0.486 g, 0.999 mmol) and 17b (0.4 g, 1.1 mmol) in pyridine (8 ml), under nitrogen, was treated with EDC (0.25 g, 1.3 mmol) and DMAP (10 mg), kept at ambient temperature for 24 h and concentrated in vacuo. A mixture of the residue in water was extracted with CH₂Cl₂; the extract was washed with saturated NaHCO₃ and brine and concentrated to give 0.6 g of 170, a yellow solid: MS (ESI−) m/z 839.4 (M+Cl).

[0464] Step 2:

[0465] A stirred suspension of 170 (0.6 g, 0.75 mmol) in DMF (5 ml), under nitrogen, was treated with piperidine (0.15 ml), kept at ambient temperature for 30 min and concentrated in vacuo. Chromatography of the solid residue on silica gel with 4% MeOH-0.2% NH₄OH—CH₂Cl₂ to 10% MeOH-0.5% NH₄OH—CH₂Cl₂ and crystallization of the product from MeOH gave 0.24 g, mp 189-190° C. and 0.06 g, mp 178-181° C. of 169: ¹H NMR [400 MHz, (CD₃)₂SO] δ 1.83 (s, 3H), 1.84 (m, 2H), 2.42 (t, 2H), 2.91, 2.95 (m, m, 4H), 3.03 (t, 2H), 3.31 (s, 2H), 3.35 (s), 3.40 (t, 2H), 3.60 (m, 4H), 3.70 (dd, 1H), 4.08 (t, 1 h), 4.71 (m, 1H), 7.06 (t, 1H), 7.18 (dd, 1H), 7.50 (dd, 1H), 7.78 (d, 2H), 7.95 (d, 2H), 8.26 (t, 1H); IR (drift) 3336, 3258, 1725, 1678, 1651, 1631 cm⁻¹; MS (ESI+) m/z 583.3 (M+H⁺); MS (ESI−) m/z 617.3 (M+Cl). Anal. calcd for C₂₉H₃₅FN₆O₆: C, 59.78; H, 6.05; N, 14.42. Found: C, 59.14; H, 6.10; N, 14.22.

Example 60 N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutyl}phenyl)-2-aminoacetamide 171.

[0466] Step 1:

[0467] A stirred mixture of 4-(4-nitrophenyl)butanoic acid (0.9 g, 4.3 mmol) and triethylamine (0.69 ml) in THF (20 ml), under nitrogen, was cooled in an ice-MeOH bath and treated, dropwise during 15 min, with isobutyl chloroformate (0.66 ml). It was kept in the bath for 50 min and the resulting thick suspension was treated with a mixture of 17b (1.44 g, 4.28 mmol), triethylamine (0.69 ml) and THF (20 ml). This mixture was kept in the ice-MeOH bath for 3 h and then mixed with EtOAc to give a mixture which contained solid product. It was washed with saturated NaHCO₃ and water and filtered to give 1.11 g of 172. The organic solution was concentrated to about 50 ml to give 0.94 g of additional product (26): MS (ESI) m/z 550.4 (M+Na⁺).

[0468] Step 2:

[0469] A mixture of 172 (1.1 g, 2.08 mmol), CH₂Cl₂ (75 ml), MeOH (75 ml) and 10% palladium-on-carbon catalyst (0.65 g) was hydrogenated for 90 min at an initial pressure of 19 psi which was raised to 50 psi during 35 min. The catalyst was removed by filtration through celite, the solid was washed with 50% MeOH—CH₂Cl₂, and the filtrate was concentrated to give 0.74 g of product. A sample of this material was chromatographed on silica gel with 5% MeOH—CHCl₃ and crystallized from MeOH-EtOAc to give 173: mp 141-143° C. (dec); MS (ESI) m/z 498.4 (M+H⁺), 520.4 (M+Na⁺); IR (drift) 3340, 3302, 3231, 1733, 1645, 1628 cm⁻¹. Anal. calcd for C₂₆H₃₂FN₅O₄: C, 62.76; H, 6.48; N, 14.07. Found: C, 62.29; H, 6.50; N, 13.85.

[0470] Step 3:

[0471] A stirred mixture of N-carbobenzyloxyglycine (0.19 g, 0.91 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 0.19 g, 0.99 mmol) and pyridine (5 ml), under nitrogen, was treated with 173 (0.43 g, 0.86 mmol) and 4-dimethylaminopyridine (DMAP, 10 mg) and kept at ambient temperature for 6 h. By TLC (0.5% NH₄OH-7.5% MeOH—CH₂Cl₂) there had been little reaction. Additional Cbz glycine (0.19 g) and EDC (0.19 g) were added and the mixture was kept at ambient temperature for 18 h. By TLC with the solvent system that contained ammonium hydroxide there still had been no reaction but TLC with 10% MeOH—CH₂Cl₂ demonstrated that the reaction was complete. The mixture was concentrated in vacuo and the residue was mixed with CH₂Cl₂ and 1N HCl to give a mixture which contained solid product. It was extracted with CH₂Cl₂ and filtered to give 0.37 g of product. The extract was washed with water and brine and concentrated. The residue was chromatographed on silica gel with 7.5% MeOH—CHCl₃ to give 0.20 g of additional product 174: MS (ESI) m/z 689.5 (M+H⁺), 711.4 (M+Na⁺).

[0472] Step 4:

[0473] A mixture of 174 (0.53 g, 0.77 mmol), MeOH (90 ml), CH₂Cl₂ (60 ml) and 10% palladium-on-carbon catalyst (0.28 g) was hydrogenated at an initial pressure of 36 psi for 7 h and filtered through celite. The solid was washed with 60% MeOH—CH₂Cl₂ and the filtrate was concentrated. Chromatography of the residue on silica gel with 0.5% NH₄OH-10% MeOH—CHCl₃ and crystallization of the product from MeOH gave 0.199 g of 171: mp 199-200° C. (dec); MS (ESI) m/z 555.4 (M+H⁺); IR (drift) 3302, 1732, 1653, 1628 cm⁻¹. Anal. calcd for C₂₈H₃₅FN₆O₅: C, 60.64; H, 6.38; N, 15.15. Found: C, 60.59; H, 6.46; N, 15.07.

Example 61 2-Amino-N-(4-{4-[4-(2-fluoro-4-{(5S)-2-oxo-5-[(propanethiolylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)-1-piperazinyl]-4-oxobutyl}phenyl)acetamide 175.

[0474] Step 1:

[0475] A stirred mixture of 4-(4-nitrophenyl)butanoic acid (0.9 g, 4.3 mmol), triethylamine (0.69 ml) and THF (20 ml), under nitrogen, was cooled in an ice-MeOH bath and treated, dropwise during 30 sec, with isobutyl chloroformate (0.66 ml). It was kept in the bath for 50 min and then treated, portionwise during 5 min, with a mixture of 17b (1.69 g, 4.28 mmol), triethylamine (0.69 ml) and THF (13 ml). This mixture was kept in the ice-methanol bath for 90 min when it was concentrated in vacuo. A mixture of the residue in CH₂Cl₂ was washed with saturated NaHCO₃, water and brine, dried (Na₂SO₄) and concentrated to give 2.54 g of 176: MS (ESI) m/z 586.5 (M+H⁺), 608.4 (M+Na⁺).

[0476] Step 2:

[0477] A mixture of 176 (1.25 g, 2.13 mmol), 10% palladium-on-carbon catalyst (0.7 g), MeOH (75 ml) and CH₂Cl₂ (75 ml) was hydrogenated at an initial pressure of 50 psi for 80 min and filtered through celite. The solid was washed with 50% MeOH—CH₂Cl₂ and the filtrate was concentrated in vacuo to give 1.17 g of 177: MS (ESI) m/z 556.5 (M+H⁺), 578.5 (M+Na⁺), 594.5 (M+K⁺).

[0478] Step 3:

[0479] A stirred mixture of N-Cbz glycine (0.50 g, 2.39 mmol) and EDC (0.46, 2.4 mmol) in pyridine (15 ml), under nitrogen, was kept at ambient temperature for 10 min and treated with 177 (0.97 g, 1.75 mmol) and DMAP (15 mg). It was kept at ambient temperature for 22 h and concentrated in vacuo. Chromatography of the residue on silica gel with 2-4% MeOH—CH₂Cl₂ gave 0.73 g (56%) of 178: MS (ESI) m/z 747.6 (M+H⁺), 769.5 (M+Na⁺).

[0480] Step 4:

[0481] A stirred suspension of 178 (0.5 g, 0.67 mmol) in dioxane (10 ml) was treated, dropwise during 4 min, with ice-cold 4N HCl in dioxane (5 ml). The mixture was cooled in an ice bath during the addition and kept in the bath for 1 h, at ambient temperature for 2 h and at 4° C. for 18 h. It was then concentrated in vacuo to give 0.50 g of 179: MS (ESI) m/z 647.6 (M+H⁺).

[0482] Step 5:

[0483] A stirred suspension of 179 (0.50 g) in MeOH (20 ml), under nitrogen, was treated with triethylamine (0.37 ml, 2.66 mmol) and ethyl dithiopropionate (0.13 ml, 1.0 mmol) and kept at ambient temperature for 22 h. It was then concentrated under a stream of nitrogen for 30 min and filtered. The solid was washed with cold MeOH and dried to give 0.30 g of 180: MS (ESI) m/z 719.6 (M+H⁺), 741.6 (M+Na⁺).

[0484] Step 6:

[0485] Solid 180 (0.28 g, 0.39 mmol) was mixed with 30% hydrogen bromide in acetic acid (3.9 ml) and stirred at ambient temperature for 30 min. The resulting solution was diluted with Et₂O (50 ml) and the liquid was decanted from the solid. This was repeated twice and the solid was then collected by filtration, washed with Et₂O, dissolved in water and made alkaline with saturated NaHCO₃. The resulting solid was collected by filtration, washed with water and dried to give 0.18 g of crude product. Additional product (0.01 g) was obtained by extracting the aqueous filtrate with CH₂Cl₂. Chromatography of the combined product on silica gel with 0.4% NH₄OH-8% MeOH—CHCl₃ and crystallization from EtOAc-MeOH gave 0.0688 g of 175: mp 161-163° C. (dec) with softening at 148° C.; MS (EST) m/z 585.5 (M+H⁺), 607.4 (M+Na⁺); IR (drift) 3322, 3256, 1753, 1749, 1744, 1727, 1681, 1631 cm⁻¹. Anal. calcd for C₂₉H₃₇FN₆O₄S: C, 59.57; H, 6.38; N, 14.37. Found: C, 58.19; H, 6.48; N, 13.85.

Example 62 (S)-2-Amino-N-(4-{4-[4-(2-fluoro-4-{(5S)-2-oxo-5-[(propanethiolylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)-1-piperazinyl]-4-oxobutyl}phenyl)propanamide 181.

[0486] Step 1:

[0487] A stirred mixture of N-carbobenzyloxy-L-alanine (0.47 g, 2.1 mmol) and EDC (0.43 g, 2.2 mmol) in pyridine (15 ml), under nitrogen, was treated with 177 (0.91 g, 1.64 mmol) and DMAP (15 mg), kept at ambient temperature for 20 h and concentrated in vacuo. Chromatography of the residue on silica gel with 2-4% MeOH—CHCl₃ gave 0.70 g of 182: MS (ESI) m/z 783.7 (M+Na⁺).

[0488] Step 2:

[0489] A stirred solution of 182 (0.57 g, 0.75 mmol) in dioxane (14 ml), under nitrogen, was treated, dropwise during 2.5 min, with ice cold 4N hydrogen chloride in dioxane (7.5 ml). The mixture was cooled in an ice bath during the addition and kept in the bath for 90 min, at ambient temperature for 4 h and at 4° C. for 16 h. Hydrogen chloride was removed under a stream of nitrogen and the resulting mixture was concentrated in vacuo to give 183, a white solid.

[0490] Step 3:

[0491] A stirred mixture of 183 from the previous reaction and triethylamine (0.37 ml) in MeOH (20 ml), under nitrogen, was treated with ethyl dithiopropionate (0.13 ml), kept at ambient temperature for 72 h and concentrated. Chromatography of the residue on silica gel with 2-3% MeOH—CHCl₃ gave 0.42 g of 184: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.12 (t, 3H), 1.26 (d, 3H), 1.77 (m, 2H), 2.32 (t, 2H), 2.55 (m, 4H), 2.90 (m, 4H), 3.56 (m, 4H), 3.78 (dd, 1H), 3.89 (t, 2H), 4.13 (m, 2H), 4.94 (m, 1H), 5.01 (s, 2H), 7.05 (t, 1H), 7.13 (m, 3H), 7.33 (m, 5H), 7.47 (m, 3H), 7.57 (d, 1H), 9.91 (s, 1H), 10.31 (t, 1H); MS (ESI) m/z 733.5 (M+H⁺), 755.5 (M+Na⁺).

[0492] Step 4:

[0493] A mixture of 184 (0.40 g, 0.55 mmol) and 30% hydrogen bromide in acetic acid (5.0 ml) was stirred for 35 min at ambient temperature and then diluted with Et₂O (100 ml). The liquid was decanted from the resulting solid which was washed twice with Et₂O, collected by filtration and washed with Et₂O. The solid was dissolved in water (20 ml) and neutralized (pH 9-10) with saturated NaHCO₃ to give a solid which was collected by filtration, dried and chromatographed on silica gel with 0.2% NH₄OH-4% MeOH—CHCl₃. The product was crystallized from MeOH to give 0.24 g of 181: MS (ESI) m/z 599.3 (M+H⁺); IR (drift) 3263, 1753, 1751, 1744, 1727, 1676, 1662, 1645, 1639, 1633 cm⁻¹; HRMS (FAB) calcd for C₃₀H₄₀FN₆O₄S (M+H⁺) 599.2816, found 599.2824. Anal. calcd for C₃₀H₃₉FN₆O₄S.0.5 H₂O: C, 59.29; H, 6.63; N, 13.83. Found: C, 59.10; H, 6.79; N, 13.59.

Example 63 N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutyl)phenyl)-2-(dimethylamino)acetamide 185.

[0494]

[0495] A stirred mixture of N,N-dimethylglycine (0.0263 g, 0.255 mmol) in pyridine (4 ml), under nitrogen, was treated with EDC (0.049 g), DMAP (5 mg) and 173 (0.127 g, 0.255 mmol), kept at ambient temperature for 3 h 10 min and concentrated in vacuo. Chromatography of the residue on silica gel with 2-6% MeOH—CH₂Cl₂ gave the product which was dissolved in CH₂Cl₂ and concentrated to give 185, a foam: MS (ESI+) m/z 583.5 (M+H⁺), 605.4 (M+Na⁺); MS (ESI−) m/z 581.4 (M−H), 617.4 (M+Cl); IR (drift) 3287, 1743, 1676, 1645 cm⁻¹; HRMS (FAB) calcd for C₃₀H₄₀FN₆O₅ (M+H⁺) 583.3044, found 583.3058.

Example 64 N-(4-{4-[4-(4-{(5S)-5-[(Ethanethiolylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutyl}phenyl)-2-(dimethylamino)acetamide 186.

[0496] Step 1:

[0497] A stirred mixture of N,N-dimethylglycine (0.028 g, 0.27 mmol) in pyridine (4 ml), under nitrogen was treated with EDC (0.052 g, 0.27 mmol), DMAP (5 mg) and 177 (0.15 g, 0.27 mmol), kept at ambient temperature for 5 h and concentrated in vacuo. Chromatography of the residue on silica gel with 2-3% MeOH—CH₂Cl₂ gave 0.09 g of 187: MS (ESI+) m/z 641.5 (M+H⁺); MS (ESI−) m/z 639.4 (M−H), 675.4 (M+Cl).

[0498] Step 2:

[0499] Compound 187 (0.21 g, 0.33 mmol) was cooled in an ice bath, under nitrogen and treated, dropwise with 4N HCl in dioxane (3.0 ml). The mixture was kept in the ice bath for 1 h and at ambient temperature for 30 min with occasional swirling. It was placed under a stream of nitrogen for 30 min and then concentrated in vacuo to give 188, a white powder: MS (ESI+) m/z 541.4 (M+H⁺); MS (ESI−) m/z 575.4 (M+Cl).

[0500] Step 3:

[0501] A stirred mixture of 188 from the previous reaction and MeOH (2.5 ml), under nitrogen was treated with triethylamine (0.4 ml) and ethyl dithioacetate (0.088 ml), kept at ambient temperature for 1 h and concentrated in vacuo. Chromatography of the residue on silica gel with 2.5-4% MeOH—CH₂Cl₂ gave 0.13 g of 186: MS (ESI+) m/z 599.4 (M+H⁺); MS (ESI−) m/z 597.3 (M−H), 633.3 (M+Cl); IR (drift) 3251, 1754, 1680, 1663, 1645, 1638 cm⁻¹; HRMS (FAB) calcd for C₃₀H₄₀FN₆O₄S (M+H⁺) 599.2816, found 599.2827.

Example 65 N¹-(3-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-1-hydroxy-4-oxobutyl}phenyl)glycinamide 189.

[0502] Step 1:

[0503] A stirred mixture of 3-nitro-□-oxo-benzenebutanoic acid,¹³ (0.9 g, 4.1 mmol) and pyridine (20 ml), under nitrogen was treated with EDC (0.96 g, 5.0 mmol), kept at ambient temperature for 2 min and treated with 17a (1.69 g, 4.29 mmol) and DMAP (20 mg). It was kept at ambient temperature for 46 h and concentrated in vacuo. A solution of the residue in CH₂Cl₂ was washed with dilute KHSO₄ and water and concentrated in vacuo. Chromatography of the residue on silica gel with 1 to 2% MeOH—CH₂Cl₂ gave 2.2 g of 190. A sample was recrystallized from EtOAc-hexane: mp 124-126° C.; ¹H NMR (300 MHz, CDCl₃) δ 1.40 (s, 9H), 2.90 (t, 2H), 3.04, 3.13 (m, m, 4H), 3.39 (t, 2H), 3.52 (m, 2H), 3.79 (m, 5H), 4.00 (t, 1H), 4.75 (m, 1H), 4.96 (m, 1H), 6.98 (t, 1H), 7.09 (dd, 1H), 7.49 (dd, 1H), 7.69 (t, 1H), 8.35 (d, 1H), 8.43 (d, 1H), 8.86 (m, 1H); MS (ESI+) m/z 599.8 (M+H⁺), 621.8 (M+Na⁺); MS (ESI−) m/z 597.8 (M−H), 633.7 (M+Cl).

[0504] Step 2:

[0505] A mixture of 190 (0.4 g, 0.67 mmol), MeOH (35 ml), CH₂Cl₂ (35 ml) and 10% palladium-on-carbon catalyst (0.2 g) was hydrogenated at an initial pressure of 29 psi for 25 min. Complete reduction of the ketone and nitro groups with little of the over reduced, deshydroxy material was obtained. The mixture was filtered through celite and the filtrate was concentrated. Chromatography of the residue over silica gel with 2 to 4% MeOH—CH₂Cl₂ gave 0.26 g of 1912: MS (ESI+) m/z 572.4 (M+H⁺), 564.4 (M+Na⁺); MS (ESI−) m/z 570.3 (M−H), 606.3 (M+Cl).

[0506] Step 3:

[0507] A stirred mixture of N-Fmoc glycine (0.45 g, 1.5 mmol) and DMF (8 ml), under nitrogen, was treated with HOBT (0.254 g) and 0.5 M DCC in CH₂Cl₂ (4.65 ml), kept at ambient temperature for 50 min and treated, dropwise, with a solution of 191 (0.88 g, 1.5 mmol) in DMF (2 ml). It was kept at ambient temperature for 90 min and concentrated in vacuo. Chromatography of the residue on silica gel with 2.5% MeOH—CH₂Cl₂ gave 0.63 g of 192: MS (ESI+) m/z 851.5 (M+H⁺), 873.5 (M+Na⁺).

[0508] Step 4:

[0509] Ice cold 4N hydrogen chloride in dioxane (4.5 ml) was added, dropwise under nitrogen, to 192 (0.65 g, 0.765 mmol) which had been cooled in an ice bath. The mixture was kept in the ice bath for 30 min and at ambient temperature for 90 min. It was then placed under a stream of nitrogen for 10 min and concentrated in vacuo to give 193, a white solid: MS (ESI+) m/z 751.5 (M+H⁺); MS (ESI−) m/z 785.2 (M+Cl).

[0510] Step 5:

[0511] An ice cold, stirred mixture of the product 193 from the previous reaction in pyridine (5 ml), under nitrogen, was treated, dropwise with a solution of acetic anhydride (1.25 ml) in pyridine (1.5 ml). It was kept in the ice bath for 40 min and at ambient temperature for 50 min and then concentrated in vacuo. A mixture of the residue in CH₂Cl₂ was washed with saturated NaHCO₃, water and brine. Concentration of the CH₂Cl₂ solution gave 0.78 g of a mixture of mono and diacylated products. A stirred mixture of this material (0.53 g) in MeOH (15 ml), under nitrogen was treated with 10% aqueous K₂CO₃ (1.8 ml) and kept at ambient temperature for 18 h. It was concentrated in vacuo. Chromatography of the residue on silica gel with 12% MeOH-0.6% NH₄OH—CH₂Cl₂ and crystallization of the product from MeOH gave 0.102 g of 189: ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.81 (s, 3H), 1.81 (m, 2H), 2.37 (t, 2H), 2.88 (m, 4H), 3.23 (s, 2H), 3.32 (broad s, 3H), 3.38 (t, 2H), 3.54 (m, 4H), 3.68 (dd, 1H), 4.06 (t, 1H), 4.52 (m, 1H), 4.69 (m, 1H), 5.26 (d, 1H), 6.98-7.25 (m, 4H), 7.45-7.56 (m, 3H), 8.23 (t, 1H); MS (ESI+) m/z 571.3 (M+H⁺), 593.3 (M+Na⁺); MS (ESI−) m/z 569.1 (M−H), 605.1 (M+Cl); IR (drift) 3444, 3372, 3342, 3307, 1749, 1680, 1663 cm⁻¹. Anal. calcd for C₂₈H₃₅FN₆O₆.2H2O: C, 55.44; H, 6.48; N, 13.85. Found: C, 54.84; H, 6.48; N, 13.60.

Example 66 N¹-[3-(4-{4-[4-((5S)-5-{[(2,2-Difluoroethanethiolyl)amino]methyl}-2-oxo-1,3-oxazolidin-3-yl)-2-fluorophenyl]piperazin-1-yl}-4-oxobutanoyl)phenol]glycinamide 194.

[0512] Step 1:

[0513] A stirred mixture of 190 (2.1 g, 3.5 mmol), cyclohexene (4 ml), 10% palladium-on-carbon catalyst (0.5 g) and EtOH (50 ml) was refluxed, under nitrogen for 2.5 h, kept at ambient temperature for 20 h, refluxed for 4 h and kept at ambient temperature for 3 d. It was then diluted with CH₂Cl₂ and filtered through celite. The solid was washed with 10% EtOAc-CH₂Cl₂ and the combined filtrate was concentrated in vacuo. Chromatography of the residue on silica gel with 3% MeOH—CH₂Cl₂ gave 195: MS (ESI+) m/z 570.4 (M+H), 592.4 (M+Na⁺).

[0514] Step 2:

[0515] A stirred mixture of N-Fmoc glycine (0.155 g, 0.521 mmol), HOBT (0.09 g) and DMF (3 ml) was treated, dropwise during 1.5 min, with 0.5 M DCC in CH₂Cl₂ (1.6 ml) and kept at ambient temperature for 50 min. It was then treated, dropwise during 2 min, with a solution of 195 (0.30 g, 0.53 mmol) in DMF (2 ml) and kept at ambient temperature for 20 h. The mixture was concentrated in vacuo and the residue was mixed with water to give a solid which was collected by filtration, washed with water and dried in vacuo. Chromatography of this material on silica gel with 7.5% MeOH—CH₂Cl₂ gave 0.42 g of 196: MS (ESI+) m/z 849.4 (M+H⁺), 871.4 (M+Na⁺); MS (ESI−) m/z 847.3 (M−H), 883.2 (M+Cl⁻).

[0516] Step 3:

[0517] Ice cold 196 (0.74 g, 0.87 mmol), under nitrogen, was treated, dropwise with ice cold 4N HCl in dioxane (6.2 ml) and the mixture was stirred in the ice bath for 30 min and at ambient temperature for 90 min. It was concentrated to give 0.72 g of 197: MS (ESI+) m/z 749.4 (M+H⁺); MS (ESI−) m/z 783.2 (M+Cl).

[0518] Step 4:

[0519] A stirred mixture of 197 (0.22 g) and triethylamine (0.08 ml) in CH₂Cl₂ (20 ml), under nitrogen, was treated, dropwise, with a solution of O-(3,3-diphenylpropyl) difluoroethanethioate (0.11 g, 0.36 mmol) in CH₂Cl₂ (0.5 ml) and kept at ambient temperature for 18 h. It was then concentrated in vacuo and the residue was chromatographed on silica gel with 3% MeOH—CH₂Cl₂ to give 198: MS (ESI+) m/z 865.3 (M+Na⁺); MS (ESI−) m/z 841.3 (M−H), 877.4 (M+Cl).

[0520] Step 5:

[0521] A stirred mixture of 198, prepared from 0.49 g of 197, in DMF (3 ml), under nitrogen, was treated with piperidine (0.10 ml), kept at ambient temperature for 40 min and concentrated in vacuo. Chromatography of the residue on silica gel with 7.5% MeOH-0.5% NH4OH—CH₂Cl₂ and crystallization of the product from MeOH-EtOAc gave 0.030 g of 194: ¹H NMR [400 MHz, (CD₃)₂SO] δ 2.76 (t, 2H), 2.92, 3.02 (s, s, 4H), 3.23 (t, 2H), 3.34 (broad s), 3.40 (s, 2H), 3.60, 3.69 (s, s, 4H), 3.84 (dd, 1H), 3.95 (m, 2H), 4.16 (t, 1H), 5.01 (m, 1H), 6.34, 6.48, 6.62 (s, s, s, 1H), 7.10 (t, 1H), 7.20 (dd, 1h), 7.48 (m, 2H), 7.70 (d, 1H), 7.89 (d, 1H), 8.25 (s, 1H); MS (ESI+) m/z 621.3 (M+H⁺); MS (ESI−) m/z 619.3 (M−H), 655.3 (M+Cl); IR (drift) 3268, 1753, 1691, 1685, 1682, 1645, 1638, 1636, 1628 cm⁻¹; HRMS (FAB) calcd for C₂₈H₃₂F₃N₆O₅S (M+H⁺) 621.2107, found 621.2117.

Example 67 N-{[(5S)-3-(3-Fluoro-4-{4-[4-(3-nitrophenyl)-4-oxobutanoyl]piperazin-1-yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}actamide 199.

[0522]

[0523] A stirred mixture of 3-nitro-□-oxo-benzenebutanoic acid,¹³ (0.9 g, 4.0 mmol) and triethylamine (0.69 ml) in THF (20 ml) was cooled, under nitrogen, in an MeOH-ice bath and treated, dropwise, with isobutyl chloroformate (0.66 ml). It was kept in the bath for 45 min and then treated, portionwise during 10 min, with a mixture of 17b¹² (1.44 g, 4.28 mmol), triethylamine (0.69 ml) and THF. The mixture was kept in the bath for 2 h and at ambient temperature for 90 min and then concentrated in vacuo. Chromatography of the residue on silica gel with 2.5% MeOH—CH₂Cl₂ and crystallization of the product from CH₃CN gave 0.69 g of 199: mp 178-179° C.; IR (drift) 3280, 1736, 1691, 1672, 1650 cm⁻¹; MS (ESI+) m/z 541.8 (M+H⁺), 563.8 (M+Na⁺); MS (ESI−) m/z 540.8 (M−H), 575.8 (M+Cl). Anal. calcd for C₂₆H₂₈FN₅O₇: C, 57.67; H, 5.21; N, 12.93. Found: C, 57.86; H, 5.33; N, 12.84.

Example 68 N¹-(3-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}phenyl)glycinamide 200.

[0524] Step 1:

[0525] A stirred mixture of 199 (0.77 g, 1.42 mmol), cyclohexene (1.0 ml), 10% palladium-on-carbon catalyst (0.21 g) and EtOH (30 ml) was refluxed, under nitrogen for 1 h and kept at ambient temperature for 18 h. Additional catalyst (0.15 g) and cyclohexene (1 ml) were added and the mixture was refluxed for 3.5 h, cooled and filtered through celite. The solid was washed with EtOH and the filtrate was concentrated to give 0.26 g of recovered 199. The solid was then washed with 50% MeOH—CH₂Cl₂ (300 ml); the filtrate was concentrated and the residue was chromatographed over silica gel with 2-4% MeOH—CH₂Cl₂. Trituration of the product with MeOH—CH₂Cl₂ gave 0.18 g of 201 as the hydrochloride salt: MS (ESI+) m/z 512.2 (M+H+), 534.2 (M+Na⁺); MS (ESI−) m/z 510.1 (M−H), 546.0 (M+Cl), 556.0 (M+HCO₂); IR (drift) several bands 3600-3400, 3355, 3281, 1738, 1682, 1662, 1632 cm⁻¹. Anal. calcd for C₂₆H₃₁ClFN₅O₅: C, 56.99; H, 5.70; N, 12.78. Found: C, 57.12; H, 6.00; N, 12.63.

[0526] Step 2:

[0527] A stirred mixture of N-Boc glycine (0.052 g, 0.29 mmol), HOBT (0.05 g), 0.5 M dicyclohexylcarbodiimide (DCC) in CH₂Cl₂ (0.9 ml) and DMF (4 ml) was kept at ambient temperature, under nitrogen, for 45 min and treated, dropwise, with a solution of 201 (0.15 g, 0.29 mmol) in DMF(2 ml). It was kept at ambient temperature for 22 h and concentrated in vacuo. Chromatography of the residue on silica gel with 5% MeOH—CHCl₃ gave 0.15 g of 202: MS (ESI+) m/z 669.3 (M+H⁺), 691.3 (M+Na⁺); MS (ESI−) m/z 667.2 (M−H).

[0528] Step 3:

[0529] Ice cold 4N HCl in dioxane (1.3 ml) was added, dropwise with stirring under nitrogen, to ice cold 202 (0.15 g, 0.22 mmol). The mixture was kept in the ice bath for 1 h and at ambient temperature for 1 h and then concentrated under a stream of nitrogen to give a white solid. This was mixed with 5% aqueous NaHCO₃ and Et₂O to give a solid. Nitrogen was bubbled through the mixture to remove the Et₂O and the solid was collected by filtration and washed with cold water. The solid was triturated with hot MeOH and recrystallized from CH₂Cl₂-MeOH to give 200: ¹H NMR [300 MHz, (CH₃)₂SO] δ 1.81 (s, 3H), 2.74 (t, 2H), 2.90, 3.00 (s, s, 4H), 3.15 (t, 2H), 3.28 (m, 4H), 3.38 (t, 2H), 3.58 (s, 2H), 3.66 (m, 3H), 4.07 (t, 1H), 4.69 (m, 1H), 7.07 (t, 1H), 7.16 (dd, 1H), 7.45 (m, 2H), 7.66 (d, 1H), 7.88 (d, 1H), 8.25 (m, 2H); IR (drift) 3316, 3287, 1748, 1702, 1682, 1662, 1630 cm⁻¹; HRMS (ESI+) calcd for C₂₈H₃₄FN₆O₆ (M+H⁺) 569.2524, found 569.2510.

Example 69 N-{[(5S)-3-(4-{4-[4-(2-Aminophenyl)-4-oxobutanoyl]piperazin-1-yl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide 203.

[0530] Step 1:

[0531] According to the method of Bianchi et.al. (Eur. J. Med. Chem. 1988, 23, 45-52) a stirred mixture of o-nitroacetophenone (2.48 g, 0.0150 mol), glyoxylic acid hydrate (1.53 g, 0.0166 mol) and acetic acid (25 ml) was treated with concentrated hydrochloric acid (2.5 ml) and warmed, under nitrogen at 125° C. for 22 h. It was then concentrated in vacuo and the residue was mixed with ice and adjusted to pH 9-10 with 10% aqueous Na₂CO₃. This mixture was washed with Et₂O, cooled and adjusted to pH 3-4 with cold dilute hydrochloric acid. The residual Et₂O was removed under a stream of nitrogen and the resulting solid was collected by filtration, washed with water, dried and crystallized from EtOH (Darco) to give 0.49 g of 204, mp 171-172° C. (lit.¹⁴ mp 169-171° C.): ¹H NMR[300 MHz, (CD₃)₂SO] δ 6.36 (d, 1H), 7.20 (d, 1h), 7.69 (dd, 1H), 7.81 (m, 1H), 7.91 (m, 1H), 8.22 (d, 1H), 13.33 (s, 1H); MS (ESI+) m/z 223.1 (M+H⁺); MS (ESI−) m/z 219.9 (M−H).

[0532] Step 2:

[0533] A stirred mixture of 204 (0.29 g, 1.3 mmol) and DMF (5 ml), under nitrogen, was treated with EDC (0.25 g, 1.3 mmol) and HOBT (0.17 g, 1.3 mmol), kept at ambient temperature for 2 min and treated with 17b (0.436 g, 1.29 mmol). It was kept at ambient temperature for 1 h and concentrated in vacuo. The residue was kept under a stream of nitrogen for 18 h and then chromatographed on silica gel with 5% MeOH—CH₂Cl₂. Crystallization of the product from EtOAc gave 0.36 g of 205: MS (ESI+) m/z 540.1 (M+H⁺), 562.1 (M+Na⁺); MS (ESI−) m/z 538.0 (M−H), 574.0 (M+Cl), 584.0 (M+CHO₂).

[0534] Step 3:

[0535] A mixture of 205 (1.18 g, 2.18 mmol), 50% MeOH—CH₂Cl₂ and 10% palladium-on-carbon catalyst was hydrogenated at an initial pressure of 40 psi for 2.25 h and filtered. The solid was washed with 50% MeOH—CH₂Cl₂ and the filtrate was concentrated to give 0.92 g, of 203. A sample which was chromatographed on silica gel with 5% MeOH-0.2% NH₄OH—CH₂Cl₂ and crystallized from MeOH had: MS (ESI+) m/z 512.4 (M+H⁺), 534.3 (M+Na⁺); MS (ESI−) m/z 510.3 (M−H), 546.2 (M+Cl); IR (drift) 3455, 3340, 3287, 1744, 1644, 1638 cm⁻¹; HRMS (FAB) calcd for C₂₆H₃₁FN₅O₅ (M+H⁺) 512.2309, found 512.2308.

Example 70 N-{[(5S)-3-(4-{4-[(5-Amino-1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)acetyl]piperazin-1-yl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide 208.

[0536] Step 1:

[0537] A stirred mixture of 4-nitrophthalic anhydride (1.4 g, 0.0072 mol), glycine (0.55 g, 0.0073 mol), sodium acetate (0.66 g, 0.0080 mol) and acetic acid (10 ml) was immersed in a bath that had been preheated to 100° C., warmed to 130° C. and kept at that temperature for 90 min. It was then kept at ambient temperature for 3 h and the thick suspension was diluted with EtOH and filtered. The solid was washed with EtOH and then crystallized from EtOH to give 2.16 g of 209: MS (ESI−) m/z 249.1 (M−H).

[0538] Step 2:

[0539] A stirred mixture of 209 (0.25 g, 1.0 mmol) and pyridine (7 ml), under nitrogen, was treated with 17b (0.34 g, 1.0 mmol), EDC (0.3 g, 1.6 mmol) and DMAP (10 mg), kept at ambient temperature for 3 h and concentrated in vacuo. Chromatography of the residue on silica gel with 5% MeOH—CH₂Cl₂ gave 0.22 g of 210: MS (ESI+) m/z 591.3 (M+Na⁺); MS (ESI−) m/z 568.2 (M−H), 603.2 (M+Cl).

[0540] Step 3:

[0541] A stirred mixture of 210 (0.5 g, 0.88 mmol), ethanol (20 ml), cyclohexene (1 ml) and 10% palladium-on-carbon catalyst (0.12 g) was refluxed, under nitrogen, for 3.5 h, diluted with CH₂Cl₂ and filtered through celite. The filtrate was concentrated in vacuo to give 0.42 g of product. A sample of this material was crystallized from MeOH-EtOAc-hexane to give 208: mp 241-243° C. (dec); MS (ESI+) m/z 539.3 (M+H⁺), 561.2 (M+Na⁺); MS (ESI−) m/z 537.2 (M−H), 573.2 (M+Cl); IR (drift) 3421, 3382, 3364, 3341, 3234, 1763, 1743, 1701, 1661 cm⁻¹; HRMS (ESI) calcd for C₂₆H₂₈FN₆O₆ (M+H⁺) 539.2054, found 539.2071.

Example 71 N¹-(2-{2-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-2-oxoethyl}-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl)glycinamide (210).

[0542] Step 1:

[0543] A stirred mixture of 208 (0.42 g, 0.78 mmol), N-Boc glycine (0.143 g, 0.817 mmol) and pyridine (6 ml), under nitrogen, was treated with EDC (0.22 g, 1.15 mmol) and DMAP (10 mg), kept at ambient temperature for 2 h 35 min and concentrated in vacuo. Chromatography of the residue on silica gel with 5% MeOH—CH₂Cl₂ gave 0.4 g of 211: ¹H NMR (300 MHz, CDCl₃) δ 1.49 (s, 9H), 2.05 (s, 3H), 3.15, 3.24 (s, s, 4H), 3.70 (m, 2H), 3.80 (m, 3H), 3.89 (s, 2H), 3.94 (d, 2H), 4.06 (t, 1H), 4.56 (s, 2H), 4.82 (m, 1H), 5.42 (m, 1H), 6.44 (t, 1H), 7.10 (m, 2H), 7.50 (d, 1H), 7.61 (d, 1H), 7.77 (d, 1H), 7.93 (s, 1H), 9.45 (s, 1H); MS (ESI+) m/z 696.3 (M+H⁺), 718.3 (M+Na⁺); MS (ESI−) m/z 694.2 (M−H), 730.1 (M+Cl).

[0544] Step 2:

[0545] A sample of 211 (0.4 g, 0.57 mmol) was cooled in an ice bath, under nitrogen and, with stirring, treated, dropwise, with 4N hydrogen chloride in dioxane (3.5 ml). It was kept in the ice bath for 30 min and at ambient temperature for 3 h and the concentrated under a stream of nitrogen. The residue was mixed with 5% NaHCO₃ and extracted with CH₂Cl₂. The extract was washed with water and brine and concentrated. Chromatography of the residue on silica gel with 6% MeOH-0.3% NH₄OH—CH₂Cl₂ to 10% MeOH-0.5% NH₄OH—CH₂Cl₂ and crystallization of the product from MeOH gave 0.133 g of 210: mp 153° C. (dec); ¹H NMR [300 MHz, (CD₃)₂SO] δ 1.84 (s, 3H), 2.96, 3.06 (s, s, 4H), 3.17 (s, 1.5H, MeOH), 3.38 (s, 2H), 3.41 (t, 2H), 3.61 (s, 2H), 3.72 (m, 3H), 4.10 (t, 1H), 4.10 (0.5H), 4.56 (s, 2H), 4.72 (m, 1H), 5.09 (broad s, 1H), 7.11 (t, 1H), 7.18 (dd, 1H), 7.52 (dd, 1H), 7.87 (d, 1 H), 7.97 (dd, 1H), 8.24 (t, 1H), 8.32 (d, 1H); IR (drift) 3369, 3300, 3217, 1758, 1744, 1714, 1712, 1662, 1646 cm⁻¹; MS (ESI+) m/z 596.3 (M+H⁺); MS (ESI−) m/z 630.1 (M+Cl). Anal. calcd for C₂₈H₃₀FN₇O₇.CH₃OH: C, 55.49; H, 5.46; N, 15.62. Found: C, 55.33; H, 5.44; N, 15.93.

Example 72 N¹-[2-(3-{4-[4-((5S)-5-{[(2,2-Difluoroethanethiolyl)amino]methyl}-2-oxo-1,3-oxazolidin-3-yl)-2-fluorophenyl]piperazin-1-yl}-3-oxopropyl)-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl)glycinamide 212.

[0546] Step 1:

[0547] A stirred mixture of 4-nitrophthalic anhydride (2.8 g, 0.0145 mol), β-alanine (1.3 g, 0.0146 mol), sodium acetate (1.32 g, 0.0161 mol) and acetic acid (20 ml) was warmed, under nitrogen to 135° C. during 90 min, kept at this temperature for 2 h and cooled to ambient temperature. It was mixed with EtOH (50 ml) and the solid was collected by filtration, washed with EtOH and dried at 55-60° C. in vacuo. Crystallization from acetonitrile gave 2.34 g, mp 210-211° C. and 0.27 g, mp 208-209° C. of 213: ¹H NMR [400 MHz, (CD₃)₂SO] δ 2.64 (t, 2H), 3.83 (t, 2H), 8.13 (d, 1H), 8.50 (d, 1H), 8.62 (dd, 1H), 12.44 (s, 1H); MS (ESI+) m/z 287.1 (M+Na⁺); MS (ESI−) m/z 263.1 (M−H).

[0548] Step 2:

[0549] A stirred mixture of 213 (1.17 g, 4.43 mmol) and pyridine (20 ml), under nitrogen was treated with EDC (1.27 g, 6.62 mmol), 17a⁵ (1.75 g, 4.44 mmol) and DMAP (20 mg), kept at ambient temperature for 19 h and concentrated in vacuo. A mixture of the residue and water was extracted with EtOAc and CH₂Cl₂. The extracts were washed with 5% NaHCO₃ and brine, dried (MgSO₄) and concentrated. Chromatography of the residue on silica gel with 2% MeOH—CH₂Cl₂ gave 2.02 g of 214: MS (ESI+) m/z 641.5 (M+H⁺), 663.5 (M+Na⁺); MS (ESI−) m/z 639.3 (M−H), 671.4 (M+CH₃O), 675.3 (M+Cl).

[0550] Step 3:

[0551] A stirred mixture of 214 (1.0 g, 1.56 mmol), cyclohexene (1.8 ml), 10% palladium-on-carbon catalyst (0.21 g) and EtOH (40 ml) was refluxed, under nitrogen for 3.25 h, cooled, diluted with CH₂Cl₂ and filtered through celite. The solid was washed with 20% EtOH-CH₂Cl₂ and the filtrates were concentrated. The residue was combined with the crude product from a second identical reaction and chromatographed on silica gel with 5% MeOH—CH₂Cl₂ to give 1.66 g of 215: ¹H NMR (400 MHz, CDCl₃) δ 1.44 (s, 9H), 2.80 (t, 2H), 3.04 (m, 4H), 3.55 (m, 2H), 3.65, 3.81 (m, m, 4H), 3.85 (m, 1H), 4.04 (m, 3H), 4.43 (s, 2H), 4.79 (m, 1H), 5.03 (m, 1H), 6.85 (dd, 1H), 6.92 (t, 1H), 7.06 (d, 1H), 7.12 (dd, 1H), 7.48 (dd, 1H), 7.63 (d, 1H); MS (ESI+) m/z 611 (M+H⁺), 633.5 (M+Na⁺); MS (ESI−) m/z 609.3 (M−H), 645.3 (M+Cl).

[0552] Step 4:

[0553] A stirred mixture of 215 (0.31 g, 0.507 mmol) and N-Fmoc glycyl chloride (0.167 g, 0.529 mmol) in THF (30 ml) was refluxed, under nitrogen for 3.5 h, cooled and concentrated in vacuo. Crystallization of the residue from MeOH-EtOAc gave 0.41 g of 216: mp 175-177° C. (dec); MS (ESI−) m/z 888.5 (M−H), 924.4 (M+35).

[0554] Step 5:

[0555] A sample of 216 (0.77 g, 0.866 mmol) was cooled in an ice bath under nitrogen and treated, dropwise with stirring during 1.5 min, with 4N hydrogen chloride in dioxane (7 ml). It was kept in the ice bath for 40 min and at ambient temperature for 110 min. Excess hydrogen chloride was removed with a stream of nitrogen and the resulting mixture was concentrated in vacuo to give 0.71 g of 217.

[0556] Step 6:

[0557] A stirred mixture of 217 (0.32 g) and triethylamine (0.11 ml) in CH₂Cl₂ (30 ml), under nitrogen was treated, dropwise, with a solution of O-(3,3-diphenylpropyl) difluoroethanethioate (0.15 g, 0.49 mmol) in CH₂Cl₂ (2 ml) and kept at ambient temperature for 4.5 h. Additional O-(3,3-diphenylpropyl) difluoroethanethioate (0.05 g) in CH₂Cl₂ (1 ml) was added and the mixture was kept at ambient temperature for 18 h and concentrated in vacuo. The residue was triturated with 3% MeOH—CH₂Cl₂ to give 0.27 g of 218: MS (ESI−) m/z 918.4 (M+Cl).

[0558] Step 7:

[0559] A stirred mixture of 14 (0.26 g, 0.294 mmol) in DMF (2 ml), under nitrogen, was treated with piperidine (0.06 ml), kept at ambient temperature for 30 min and concentrated in vacuo. Chromatography of the residue on silica gel with 5% MeOH-0.3% NH₄OH—CH₂Cl₂ to 7.5% MeOH-0.5% NH₄OH—CH₂Cl₂ gave 0.032 g of 101: MS (ESI+) m/z 662.3 (M+H⁺); MS (ESI−) m/z 696.3 (M+Cl); IR (drift) 3241, 1749, 1744, 1710, 1677, 1663, 1645, 1628; HRMS calcd for C₂₉H₃₁F₃N₇O₆S (M+H⁺) 662.2008, found 662.2029.

Example 73 MIC Test Method

[0560] The in vitro MICs of test compounds were determined by a standard agar dilution method. A stock drug solution of each analog was prepared in the preferred solvent, usually DMSO:H₂O (1:3). Serial 2-fold dilutions of each sample are made using 1.0 ml aliquots of sterile distilled water. To each 1.0 ml aliquot of drug was added 9 ml of molten Mueller Hinton agar medium. The drug-supplemented agar was mixed, poured into 15×100 mm petri dishes, and allowed to solidify and dry prior to inoculation.

[0561] Vials of each of the test organisms are maintained frozen in the vapor phase of a liquid nitrogen freezer. Test cultures are grown overnight at 35° C. on the medium appropriate for the organism. Colonies are harvested with a sterile swab, and cell suspensions are prepared in Trypticase Soy broth (TSB) to equal the turbidity of a 0.5 McFarland standard. A 1:20 dilution of each suspension was made in TSB. The plates containing the drug supplemented agar are inoculated with a 0.001 ml drop of the cell suspension using a Steers replicator, yielding approximately 10⁴ to 10⁵ cells per spot. The plates are incubated overnight at 35° C.

[0562] Following incubation the Minimum Inhibitory Concentration (MIC μg/ml), the lowest concentration of drug that inhibits visible growth of the organism, was read and recorded. The data is shown in Table I. TABLE 1 MIC Data^(a) Compound SAUR^(b) SAUR SEPI^(c) EFAE^(d) EFAE^(e) SPNE^(f) SPYO^(g) HINF^(h) HINF MCAT^(i) No. Structure 9213 31583 30593 9217 12712 9912 152 30063 31810 30607 2

2 4 1 1 1 0.125 0.125 16 8 2 8

32 >64 8 32 32 2 2 >64 >64 32 9

4 32 2 2 2 0.25 0.25 32 32 4 10

2 8 1 2 2 0.25 0.25 32 32 2 13

8 16 1 1 2 0.125 0.25 16 16 4 14

16 >64 8 8 8 0.5 0.5 64 32 32 17

8 32 2 1 2 0.25 0.5 64 32 4 18

4 16 1 1 2 0.25 0.25 64 32 2 19

16 >64 8 4 8 1 1 >64 64 64 22

8 32 2 2 0.125 0.25 32 16 2 23

16 >64 8 8 0.5 0.5 64 64 32 24

4 16 2 2 0.125 0.25 32 16 2 

We claim:
 1. A compound of formula I

or pharmaceutically acceptable salts thereof wherein: A is a structure i, ii, iii, or iv;

W is —N(H)C(X)—R₁, Het, or —Y—HET, in which the Het or —Y—HET is optionally substituted with ═S or ═O, provided that when A is structure iv, W is not —Y—HET or Het; X is O or S; Y is NH, O, or S; Z is

R₁ is a) H, b) NH₂, c) NHC₁₋₄alkyl, d) C₁₋₄alkyl, e) C₂₋₄alkenyl, f) O—C₁₋₄alkyl, i) S-C₁₋₄alkyl, or j) (CH₂)_(s) C₃₋₆ cycloalkyl, in which each occurrence of alkyl or cycloalkyl in R₁ is optionally substituted by one, two or three halogens (F or Cl); Each R₂ and R₃ is independently hydrogen, halogen (F or Cl), methyl or ethyl; R₄ is H, CH₃ or F; R₅ is H or C₁₋₄alkyl; R₆ is H, C₁₋₄ alkyl, or

or R₅ and R₆ together form an optionally substituted saturated heterocycle; R₇ is H, or C₁₋₄ alkyl which can be optionally substituted by —OH, —NH₂, —NH—C(═NH)—NH₂, —SH, —SCH₃, —COOH, —C(O)NH₂, phenyl which can be optionally substituted with —OH; R₈ is H or CH₃; R₉ is H, CH₃, —C(O)—CH(R₇)—NR₈R₈,

R₁₀ or R₁₁ is halo, C₁₋₄alkyl, CF₃, —CN, —NO₂, —OH, —O—C₁₋₄alkyl, —NH—S(O)_(w)C₁₋₄alkyl;

R₁₂ is H, C₁₋₄alkyl, —S(O)₂—C₁₋₄alkyl,

or R₅ and R₁₂ together form a saturated heterocycle; R₁₃ is H, or

R₁₄ is —(CH₂)_(t)NHR₁₃, —OH, —OC₁₋₄alkyl; m is 0, 1, 2, 3, 4; n is 0, 1, 2, 3, 4 with the proviso that m plus n is 2, 3, 4, or 5; p is 2, 3; q is 1, 2; r, s and t are independently 0, 1; u and w are independently 0, 1, 2; and provided that W is not Het or —Y—HET when Z is a, b, or d, and further provided that Z is not b when A is formula iii.
 2. The compound of claim 1, wherein B is


3. The compound of claim 2, wherein p is
 2. 4. The compound of claim 1, wherein B is


5. The compound of claim 4, wherein n and m are both
 2. 6. The compound of claim 4, wherein n and m are both
 1. 7. The compound of claim 4, wherein R₄ is —CH₃.
 8. The compound of claim 2, wherein Z is (a).
 9. The compound of claim 8, wherein R₅ and R₆ are C₁₋₄ alkyl.
 10. The compound of claim 8, wherein R₅ and R₆ together form an optionally substituted saturated heterocycle.
 11. The compound of claim 10, wherein R₅ and R₆ form an optionally substituted morpholinyl and piperazinyl.
 12. The compound of claim 11, wherein R₅ and R₆ form a morpholinyl and piperazinyl each of which are substituted with C₁₋₄ alkyl.
 13. The compound of claim 8, wherein u=0.
 14. The compound of claim 4, wherein Z is (a).
 15. The compound of claim 14, wherein R₅ and R₆ are C₁₋₄ alkyl.
 16. The compound of claim 14, wherein R₅ and R₆ together form an optionally substituted saturated heterocycle.
 17. The compound of claim 16, wherein R₅ and R₆ form an optionally substituted morpholinyl and piperazinyl.
 18. The compound of claim 17, wherein R₅ and R₆ form a morpholinyl and piperazinyl each of which are substituted with C₁₋₄ alkyl.
 19. The compound of claim 14, wherein u=0.
 20. The compound of claim 2, wherein Z is (c).
 21. The compound of claim 20, wherein R₁₀ is H.
 22. The compound of claim 20, wherein R₁₁ is —C(O)—NH₂, —NHS(O)_(u)C₁₋₄alkyl, or —(CH₂)_(t)—NR₅R₁₂.
 23. The compound of claim 22, wherein R₁₁ is —CH₂N(C₁₋₄alkyl)₂, —CH₂— satrurated heterocycle, —CH₂—NH—C₁₋₄alkyl, —CH₂—N(C₁₋₄alkyl)-C(O)—CHR₇—NR₈R₉, —CH₂—NH—C(O)—C₁₋₄alkyl, —CH₂—NH—SO₂—(C1-4alkyl), —CH₂—NH₂, or —NH—C(O)—CHR₇—NR₈R₉.
 24. The compound of claim 20, wherein R₁₀ is ortho to R₁₁.
 25. The compound of claim 20, wherein q is
 1. 26. The compound of claim 4, wherein Z is (c).
 27. The compound of claim 26, wherein R₁₀ is H.
 28. The compound of claim 26, wherein R₁₁ is —C(O)—NH₂, —NHS(O)_(u)C₁₋₄alkyl, or —(CH₂)_(t)—NR₅R₁₂.
 29. The compound of claim 28, wherein R₁₁ is —CH₂N(C₁₋₄alkyl)₂, —CH₂— satrurated heterocycle, —CH₂—NH—C₁₋₄alkyl, —CH₂—N(C1-4alkyl)-C(O)—CHR₇—NR₈R₉, —CH₂—NH—C(O)—C₁₋₄alkyl, —CH₂—NH—SO₂—(C1-4alkyl), —CH₂—NH₂, or —NH—C(O)—CHR₇-NR₈R₉.
 30. The compound of claim 26, wherein q is
 1. 31. The compound of claim 2, wherein Z is (b).
 32. The compound of claim 31, wherein R₁₄ is —OC₁₋₄ alkyl, —OH, or —NH—C(O)—CH(R₇)—NR₈R₉.
 33. The compound of claim 4, wherein Z is (b).
 34. The compound of claim 33, wherein R₁₄ is —OC₁₋₄ alkyl, —OH, or —NH—C(O)—CH(R₇)—NR₈R₉.
 35. The compound N-[((5S)-3-{4-[4-({4-[(Diethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide; N-[((5S)-3-{4-[4-({4-[(Diethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]cyclopropanecarbothioamide; N-[((5S)-3-{4-[4-({4-[(Diethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide; N-[((5S)-3{4-[4-({4-[(Dimethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide; N-[((5S)-3-{4-[4-({4-[(Dimethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]cyclopropanecarbothioamide; N-[((5S)-3-{4-[4-({4-[(Dimethylamino)methyl]phenoxy}acetyl)piperazin-1-yl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide; N-({(5S)-3-[3-Fluoro-4-(4-{[4-(morpholin-4-ylmethyl)phenoxy]acetyl}piperazin-1-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)propanethioamide; N-({(5S)-3-[3-Fluoro-4-(4-{[4-(morpholin-4-ylmethyl)phenoxy]acetyl}piperazin-1-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)cyclopropanecarbothioamide; N-({(5S)-3-[3-Fluoro-4-(4-{[4-(morpholin-4-ylmethyl)phenoxy]acetyl}piperazin-1-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide; N-[((5S)-3-{3-Fluoro-4-[4-({4-[(4-methylpiperazin-1-yl)methyl]phenoxy}acetyl)piperazin-1-yl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide; N-[((5S)-3-{3-Fluoro-4-[4-({4-[(4-methylpiperazin-1-yl)methyl]phenoxy}acetyl)piperazin-1-yl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]cyclopropanecarbothioamide; N-[((5S)-3-{3-Fluoro-4-[4-({4-[(4-methylpiperazin-1-yl)methyl]phenoxy}acetyl)piperazin-1-yl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide; N-[((5S)-3-{4-[4-(4-{4-[(Dimethylamino)methyl]phenyl}-4-oxobutanoyl)-1-piperazinyl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide; N-[((5S)-3-{4-[4-(4-{4-[(Dimethylamino)methyl]phenyl}-4-oxobutanoyl)-1-piperazinyl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]cyclopropanecarbothioamide; N-[((5S)-3-{4-[4-(4-{4-[(Dimethylamino)methyl]phenyl}-4-oxobutanoyl)-1-piperazinyl]-3-fluorophenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide; N-({(5S)-3-[3-Fluoro-4-(4-{4-[4-(4-morpholinylmethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)propanethioamide; N-({(5S)-3-[3-Fluoro-4-(4-{4-[4-(4-morpholinylmethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide; N-({(5S)-3-[3-Fluoro-4-(4-{4-[4-(4-morpholinylmethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)cyclopropanecarbothioamide; N-[((5S)-3-{3-Fluoro-4-[4-(4-{4-[(methylamino)methyl]phenyl}-4-oxobutanoyl)piperazin-1-yl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide; N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-piperazin-1-yl]-4-oxobutanoyl}benzyl-N¹-methylglycinamide; N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)-N¹,N²,N²-trimethylglycinamide; N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)-N²,N²-dimethylglycinamide; N¹-(4-{4-[4-[2-Fluoro-4-{(5S)-2-oxo-5-[(propanethiolylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)-N²,N²-dimethylglycinamide; (S)-N¹-(4-{4-[4-(2-Fluoro-4-{(5S)-2-oxo-5-[(propanethioylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)alaninamide; (S)-N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-2-oxobutanoyl}benzyl)alaninamide; N¹-(4-{4-[4-(2-Fluoro-4-{(5S)-2-oxo-5-[(propanethioylamino)methyl]-1,3-oxazolidan-3-yl}phenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)glycinamide; (S)-Alanyl-(S)-N¹-(4-{4-[4-(2-fluoro-4-{(5S)-2-oxo-5-[(propanethioylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)alaninamide; (S)-Alanyl-(S)-N¹-(4-{4-[4-(4-{(5S)-5-[(acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)alaninamide; N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}benzyl)acetamide; N-(4-{4-[4-(2-Fluoro-4-{(5S)-2-oxo-5-[(propanethioylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)-1-piperazinyl]-4-oxobutanoyl}benzyl)acetamide; N-{[(5S)-3-(3-Fluoro-4-{4-[4-(4-{[(methylsulfonyl)amino]methyl}phenyl)-4-oxobutanoyl]-1-piperazinyl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide; N-{[(5S)-3-(3-Fluoro-4-{4-[4-(4-{[(methylsulfonyl)amino]methyl}phenyl)-4-oxobutanoyl]-1-piperazinyl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}propanethioamide; N-({(5S)-3-[4-(4-{4-[4-(Aminomethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl)-3-fluorophenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)propanethioamide; N-({(5S)-3-[4-(4-{4-[4-(Aminomethyl)phenyl]-4-oxobutanoyl}-1-piperazinyl-3-fluorophenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide; N¹-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}benzyl)glycinamide; 2-[3-methyl-3-(4-{(5S)-2-oxo-5-[(propionylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)azetidin-1-yl]-2-oxoethyl4-(aminomethyl)benzamide; N-{[(5S)-3-(4-{1-[4-(4-aminophenyl)-4-oxobutanoyl]-3-methylezetidin-3-yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}propanamide; N-({(5S)-3-[4-(1-{4-[4-(glycylamino)phenyl]-4-oxobutanoyl}-3-methylazetidin-3-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)propanamide; N-{[(5S)-3-(4-{1-[4-(4-aminophenyl)-4-oxobutanoyl]-3-methylazetidin-3-yl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide; N˜1˜-(4-{4-[3-(4-{(5S)-5-[(acetylamino)methyl]-2-oxo-1,3-oxozolidin-3-yl}-2-fluorophenyl)-3-methylazetidin-1-yl]-4-oxobutanoyl}phenyl)glycinamide; 2-[3-(4-{(5S)-5-[(acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-3-methylazetidin-1-yl]-2-oxoethyl-4-(aminomethyl)benzamide; N-{[(5S)-3-(3-Fluoro-4-{4-[4-(4-methoxyphenyl)butanoyl]piperazine-1-yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide; N-{[(5S)-3-(3-Fluoro-4-{4-[4-(4-hydroxyphenyl)butanoyl]piperazin-1-yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide; 2,2-Difluoro-N-{[(5S)-3-(3-fluoro-4-{4-[4-(4-methoxyphenyl)butanolyl]piperazin-1-yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}ethanethioamide; N-{[(5S)-3-(4-{4-[4-(4-Bromophenyl)-4-oxobutanoyl]-1-piperazinyl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide; N-{[(5S)-3-(4-{4-[4-(4-Bromophenyl)-4-oxobutanoyl]-1-piperazinyl]-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}ethanethioamide; N-{[(5S)-3-(4-{4-[4-(4-Cyanophenyl)-4-oxobutanoyl]-1-piperazinyl}-3-fluorophenyl-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide; 4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}benzamide; 4-{4-[4-(4-{(5S)-5-[(Ethanethiolylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}benzamide; N-{[(5S)-3-(4-{4-[4-(4-Chlorophenyl)-4-oxobutanoyl]-1-piperazinyl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide; N-{[(5S)-3-(4-{4-[4-(4-chlorophenyl)-4-oxobutanoyl]-1-piperazinyl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}ethanethioamide; N-[((5S)-3-{3-Fluoro-4-[4-(4-{4-[(methylsulfonyl)amino]phenyl}-4-oxobutanoyl)-1-piperazinyl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]propanethioamide; N-[((5S)-3-{3-Fluoro-4-[4-(4-{4-[(methylsulfonyl)amino]phenyl}-4-oxobutanoyl-1-piperazinyl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]acetamide. N-(4-{4-[4-(2-Fluoro-4-{(5S)-2-oxo-5-[(propanethiolylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)-1-piperazinyl]-4-oxobutanoyl}phenyl)acetamide; 2-Amino-N-(4-{4-[4-(2-fluoro-4-{(5S)-2-oxo-5-[(propanethioylamino)methyl]1,3-oxazolidin-3-yl}phenyl)-1-piperazinyl]-4-oxobutanoyl}phenyl)acetamide; N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}phenyl)-2-aminoacetamide; N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutanoyl}phenyl)-(2S)-2-aminopropanamide; N-1-(4-{4-[4-(4-{(5S)-5-[(Ethanethiolylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}phenyl)-(S)-alaninamide; N¹-[4-(5-{4-[4-((5S)-5-{[(2,2-Difluoroethanethioyl)amino]methyl}-2-oxo-1,3-oxazolidin-3-yl)-2-fluorophenyl]piperazin-1-yl}-5-oxopentanoyl)phenyl]glycinamide; N¹-(4-{5-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-5-oxopentanoyl}phenyl)glycinamide; N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)-1-piperazinyl]-4-oxobutyl}phenyl)-2-aminoacetamide; 2-Amino-N-(4-{4-[4-(2-fluoro-4-{(5S)-2-oxo-5-[(propanethiolylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)-1-piperazinyl]-4-oxobutyl}phenyl)acetamide; (S)-2-Amino-N-(4-{4-[4-(2-fluoro-4-{(5S)-2-oxo-5-[(propanethiolylamino)methyl]-1,3-oxazolidin-3-yl}phenyl)-1-piperazinyl]-4-oxobutyl}phenyl)propanamide; N-(4-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutyl)phenyl)-2-(dimethylamino)acetamide; N-(4-{4-[4-(4-{(5S)-5-[(Ethanethiolylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutyl}phenyl)-2-(dimethylamino)acetamide; N¹-(3-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-1-hydroxy-4-oxobutyl}phenyl)glycinamide; N¹-[3-(4-{4-[4-((5S)-5-{[(2,2-Difluoroethanethiolyl)amino]methyl}-2-oxo-1,3-oxazolidin-3-yl)-2-fluorophenyl]piperazin-1-yl}-4-oxobutanoyl)phenyl]glycinamide; N-{[(5S)-3-(3-Fluoro-4-{4-[4-(3-nitrophenyl)-4-oxobutanoyl]piperazin-1-yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}actamide; N¹-(3-{4-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-4-oxobutanoyl}phenyl)glycinamide; N-{[(5S)-3-(4-{4-[4-(2-Aminophenyl)-4-oxobutanoyl]piperazin-1-yl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide; N-{[(5S)-3-(4-{4-[(5-Amino-1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)acetyl]piperazin-1-yl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide; N¹-(2-{2-[4-(4-{(5S)-5-[(Acetylamino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenyl)piperazin-1-yl]-2-oxoethyl}-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl)glycinamide; or N¹-[2-(3-{4-[4-((5S)-5-{[(2,2-Difluoroethanethiolyl)amino]methyl}-2-oxo-1,3-oxazolidin-3-yl)-2-fluorophenyl]piperazin-1-yl}-3-oxopropyl)-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl)glycinamide.
 36. A method for the treatment of microbial infections in mammals comprising administration of an effective amount of compound of claim 1 to said mammal.
 37. The method of claim 36 wherein said compound of claim 1 is administered to the mammal orally, parenterally, transdermally, or topically in a pharmaceutical composition.
 38. The method of claim 37 wherein said compound is administered in an amount of from about 0.1 to about 100 mg/kg of body weight/day.
 39. The method of claim 37 wherein said compound is administered in an amount of from about 1 to about 50 mg/kg of body weight/day.
 40. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier. 